ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563685
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000417903
RCV000420631
RCV000423140
RCV000424403
RCV000425922
RCV000430027
RCV000430739
RCV000432539
RCV000435554
RCV000436172
RCV000438282
RCV000440264
RCV000443104
RCV000443133
RCV000443946
RCV003621531
ClinVar Variation:
376592
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Glu127Val
CA16603014
NM_001276698.3:c.380A>T