Canonical Allele Identifier: PA2825580041
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108451.1:p.Arg319Cys
CA118338
NM_001114979.2:c.955C>T