Canonical Allele Identifier: PA645501130
Gene: BAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 412422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004647.1:p.Ala574Val
CA2436751
NM_004656.4:c.1721C>T