Canonical Allele Identifier: PA2827265486
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 653417
ClinVar RCV Id: RCV000809190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Asn152Lys
CA355753768
NM_001329149.2:c.456C>G
CA355753770
NM_001329149.2:c.456C>A