Canonical Allele Identifier: PA2827281583
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg317Cys
CA118338
NM_001329964.2:c.949C>T