Canonical Allele Identifier: PA2827265423
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6537
ClinVar RCV Id: RCV000006911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.Asn6His
CA340597
NM_001329149.2:c.16A>C