Canonical Allele Identifier: PA2580308730
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450420
ClinVar RCV Id: RCV003176933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.His563Pro
CA353099842
NM_004656.4:c.1688A>C