Canonical Allele Identifier: PA913195182
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620598
ClinVar RCV Id: RCV000761021 RCV000774726 RCV000797507 RCV001566382 RCV003411701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Glu611Asp
CA2436706
NM_004656.4:c.1833G>C
CA353098334
NM_004656.4:c.1833G>T