Canonical Allele Identifier: PA658820054
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539906
ClinVar RCV Id: RCV000649776 RCV001775940 RCV001805780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Pro588Arg
CA2436720
NM_004656.4:c.1763C>G