Allele Registry

Canonical Allele Identifier: PA093698

Gene: SLC6A2 HGNC NCBI

ClinVar RCV:

RCV000015043

ClinVar Variation:

14006

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034.1:p.Ala457Pro	CA123699 NM_001043.3:c.1369G>C