Canonical Allele Identifier: PA2827264500
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 478110
ClinVar RCV Id: RCV000559680 RCV000851194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.His153Tyr
CA355753773
NM_001329145.2:c.457C>T