Canonical Allele Identifier: PA915980023
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro58Ser
CA397840839
NM_001126117.1:c.172C>T