Canonical Allele Identifier: PA891847498
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 575932
ClinVar RCV Id: RCV000698285 RCV000774732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Arg540His
CA2436769
NM_004656.4:c.1619G>A