Canonical Allele Identifier: PA913195182
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Glu611Asp
CA2436706
NM_004656.4:c.1833G>C
CA353098334
NM_004656.4:c.1833G>T