Canonical Allele Identifier: PA2827264467
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719227
ClinVar RCV Id: RCV002301987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Val121Leu
CA355753331
NM_001329145.2:c.361G>C
CA355753332
NM_001329145.2:c.361G>T