Canonical Allele Identifier: PA2827265462
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 730540
ClinVar RCV Id: RCV001513730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Ile131Val
CA2752223
NM_001329149.2:c.391A>G