Allele Registry

Canonical Allele Identifier: PA2829886804

Gene: VPS13D HGNC NCBI

ClinVar RCV:

RCV000680233

ClinVar Variation:

561203

HGVS (amino-acid)	Matching Registered Transcripts
NP_060626.2:p.Asn3496Ser	CA338498310 NM_018156.4:c.10487A>G