Canonical Allele Identifier: PA2827265712
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6529
ClinVar RCV Id: RCV000006902
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.Cys166Arg
CA118336
NM_001329150.2:c.496T>C