Canonical Allele Identifier: PA2827264674
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719227
ClinVar RCV Id: RCV002301987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Val36Leu
CA355753331
NM_001329146.2:c.106G>C
CA355753332
NM_001329146.2:c.106G>T