Canonical Allele Identifier: PA157261
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133666
ClinVar RCV Id: RCV000120194 RCV000229762 RCV000573314 RCV000657094 RCV003965007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Gly579Arg
CA157259
NM_004656.4:c.1735G>A
CA353099337
NM_004656.4:c.1735G>C