Canonical Allele Identifier: PA2827264204
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2703814
ClinVar RCV Id: RCV003592564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Pro219Leu
CA355753377
NM_001329144.2:c.656C>T