Canonical Allele Identifier: PA2827264481
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 444621
ClinVar RCV Id: RCV000512665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Lys139Thr
CA355753628
NM_001329145.2:c.416A>C