ClinGen Allele Registry
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Canonical Allele Identifier:
PA645436130
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
245074
ClinVar RCV:
RCV000235329
RCV000417778
RCV000418017
RCV000418929
RCV000421969
RCV000422641
RCV000423061
RCV000424499
RCV000426785
RCV000427794
RCV000429015
RCV000429222
RCV000433090
RCV000433333
RCV000434308
RCV000435664
RCV000438017
RCV000439251
RCV000439625
RCV000439855
RCV000440307
RCV000442812
RCV000444463
RCV000574439
RCV000704159
RCV000785238
RCV002268012
RCV003152698
RCV003483596
ClinVar Variation:
245851
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119589.1:p.Arg43Cys
CA002442
NM_001126117.1:c.127C>T