Canonical Allele Identifier: PA658725292
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 489625
ClinVar RCV Id: RCV000580478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser585Tyr
CA353099214
NM_004656.4:c.1754C>A