Canonical Allele Identifier: PA2827264565
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208418
ClinVar RCV Id: RCV000190455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Ala252Gly
CA204448
NM_001329145.2:c.755C>G