Canonical Allele Identifier: PA658673366
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 485290
ClinVar RCV Id: RCV000569781 RCV001072025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Glu620Lys
CA2436698
NM_004656.4:c.1858G>A