Canonical Allele Identifier: PA2829554816
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3224441
ClinVar RCV Id: RCV004519167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Glu602Gln
CA353098714
NM_004656.4:c.1804G>C