Allele Registry

Canonical Allele Identifier: PA658828798

Gene: VPS13D HGNC NCBI

ClinVar RCV:

RCV000680233

ClinVar Variation:

561203

HGVS (amino-acid)	Matching Registered Transcripts
NP_056193.2:p.Asn3521Ser	CA338498310 NM_015378.4:c.10562A>G