Canonical Allele Identifier: PA2827265197
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 431904
ClinVar RCV Id: RCV000497878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Arg338His
CA89746661
NM_001329148.2:c.1013G>A