Canonical Allele Identifier: PA2826567363
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 659457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ile215Ser
CA397837758
NM_001276761.3:c.644T>G