Canonical Allele Identifier: PA645436002
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser314Phe
CA001234
NM_001126114.3:c.941C>T