Canonical Allele Identifier: PA2580308772
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782066
ClinVar RCV Id: RCV002408021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Lys630Asn
CA353097838
NM_004656.4:c.1890G>T
CA353097840
NM_004656.4:c.1890G>C