Canonical Allele Identifier: PA2827264299
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208418
ClinVar RCV Id: RCV000190455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Ala346Gly
CA204448
NM_001329144.2:c.1037C>G