Canonical Allele Identifier: PA2830316227
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1491704
ClinVar RCV Id: RCV001988838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Thr2426Ala
CA371875596
NM_152564.5:c.7276A>G