Canonical Allele Identifier: PA2827264764
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 431904
ClinVar RCV Id: RCV000497878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg159His
CA89746661
NM_001329146.2:c.476G>A