Allele Registry

Canonical Allele Identifier: PA2829812406

Gene: VPS13A HGNC NCBI

ClinVar Variation Id: 367392

HGVS (amino-acid)	Matching Registered Transcripts
NP_056001.1:p.Asn1929Ser	CA5092850 NM_015186.4:c.5786A>G