Canonical Allele Identifier: PA2741918138
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2975840
ClinVar RCV Id: RCV003833926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser596Arg
CA353098850
NM_004656.4:c.1788C>G
CA353098856
NM_004656.4:c.1788C>A
CA353098879
NM_004656.4:c.1786A>C