Canonical Allele Identifier: PA2829811671
Gene: VPS13A HGNC NCBI

Linked Data

ClinVar Variation Id: 367364
ClinVar RCV Id: RCV000347795 RCV000518783 RCV001562536 RCV002523807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056001.1:p.Ser734Asn
CA5091890
NM_015186.4:c.2201G>A