Canonical Allele Identifier: PA2741918102
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2792339
ClinVar RCV Id: RCV003643272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Arg540Gly
CA353100285
NM_004656.4:c.1618C>G