Allele Registry

Canonical Allele Identifier: PA108056

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022332

RCV000186137

RCV002226449

ClinVar Variation:

38279

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Ala214Val	CA312942 NM_003060.4:c.641C>T