Canonical Allele Identifier: PA2825611280
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Cys143Trp
CA397836936
NM_001126115.1:c.429T>G