Canonical Allele Identifier: PA2580308588
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1769592
ClinVar RCV Id: RCV002381030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Leu437Met
CA353102198
NM_004656.4:c.1309C>A