ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645436162
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376606
ClinVar RCV Id:
RCV000420789
RCV000417695
RCV000427175
RCV000417973
RCV000421853
RCV000423292
RCV000433943
RCV000437826
RCV000426502
RCV000433227
RCV000428674
RCV000429260
RCV000443785
RCV000438042
RCV000438407
RCV000439947
RCV000432550
RCV000440632
RCV000529132
RCV000445268
RCV000785555
RCV001023983
RCV001591055
RCV003983035
RCV004022216
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119589.1:p.His47Arg
CA16603027
NM_001126117.1:c.140A>G