Canonical Allele Identifier: PA1139734044
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 922537
ClinVar RCV Id: RCV001182656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ser628Ala
CA353097912
NM_004656.4:c.1882T>G