Canonical Allele Identifier: PA2741969206
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 3002945
ClinVar RCV Id: RCV003860536
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061138.3:p.Ala2Val
CA274765057
NM_018668.5:c.5C>T