Allele Registry

Canonical Allele Identifier: PA645463667

Gene: VPS13A HGNC NCBI

ClinVar RCV:

RCV000368612

RCV000861046

RCV001579965

RCV003922655

ClinVar Variation:

367413

HGVS (amino-acid)	Matching Registered Transcripts
NP_150648.2:p.Ile2486Thr	CA5093361 NM_033305.3:c.7457T>C