Canonical Allele Identifier: PA2741918099
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626737
ClinVar RCV Id: RCV003384277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Leu539Val
CA353100293
NM_004656.4:c.1615C>G