Canonical Allele Identifier: PA2827264780
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Asp172Gly
CA118341
NM_001329146.2:c.515A>G