Allele Registry

Canonical Allele Identifier: PA645507285

Gene: SLC18A3 HGNC NCBI

ClinVar RCV:

RCV000412646

ClinVar Variation:

372160

HGVS (amino-acid)	Matching Registered Transcripts
NP_003046.2:p.Asp398His	CA16042222 NM_003055.3:c.1192G>C