Canonical Allele Identifier: PA2741918044
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2824683
ClinVar RCV Id: RCV003643879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser469Arg
CA353101530
NM_004656.4:c.1407C>G
CA353101533
NM_004656.4:c.1407C>A
CA353101552
NM_004656.4:c.1405A>C