Canonical Allele Identifier: PA2741905362
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2721206
ClinVar RCV Id: RCV003592908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Ala554Val
CA2752549
NM_003722.5:c.1661C>T