Canonical Allele Identifier: PA2827264278
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Arg319Cys
CA118338
NM_001329144.2:c.955C>T