Canonical Allele Identifier: PA111719
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg319Cys
CA118338
NM_003722.5:c.955C>T