Canonical Allele Identifier: PA2827265206
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 418520
ClinVar RCV Id: RCV000481657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Cys347Phe
CA16617858
NM_001329148.2:c.1040G>T