Canonical Allele Identifier: PA2827265200
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 279913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Arg343Trp
CA10602901
NM_001329148.2:c.1027C>T