Canonical Allele Identifier: PA169162
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12382
ClinVar RCV Id: RCV000013182 RCV000144671 RCV000536677 RCV001192620 RCV000132058 RCV001030736 RCV003476892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Ala57Val
CA000270
NM_001126115.1:c.170C>T