Canonical Allele Identifier: PA658673311
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472668
ClinVar RCV Id: RCV000539926 RCV002395450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ala471Val
CA74740824
NM_004656.4:c.1412C>T