Canonical Allele Identifier: PA1139733849
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 924328
ClinVar RCV Id: RCV001185615 RCV002304234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Gln590His
CA353098995
NM_004656.4:c.1770A>T
CA353098998
NM_004656.4:c.1770A>C