Canonical Allele Identifier: PA2741918135
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3029581
ClinVar RCV Id: RCV003896681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Pro588Ser
CA353099105
NM_004656.4:c.1762C>T