Canonical Allele Identifier: PA2827264695
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2849003
ClinVar RCV Id: RCV003757724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Thr59Met
CA89742094
NM_001329146.2:c.176C>T