Canonical Allele Identifier: PA2826564479
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 234067
ClinVar Variation Id: 428879
ClinVar RCV Id: RCV000492463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asn151Lys
CA10580910
NM_001276699.3:c.453C>A
CA397836109
NM_001276699.3:c.453C>G