Canonical Allele Identifier: PA1139734244
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834924
ClinVar RCV Id: RCV001035708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Thr668Ser
CA353096330
NM_004656.4:c.2003C>G
CA353096332
NM_004656.4:c.2002A>T