Canonical Allele Identifier: PA2826566108
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser264Asn
CA10580912
NM_001276760.3:c.791G>A