Canonical Allele Identifier: PA2827281598
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 279913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg341Trp
CA10602901
NM_001329964.2:c.1021C>T