Canonical Allele Identifier: PA2827264561
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 279913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Arg249Trp
CA10602901
NM_001329145.2:c.745C>T