Canonical Allele Identifier: PA2573241689
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418046
ClinVar RCV Id: RCV001951937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Thr576Pro
CA353099524
NM_004656.4:c.1726A>C