Allele Registry

Canonical Allele Identifier: PA108066

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001975156

ClinVar Variation:

1459138

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Ala301Asp	CA342664 NM_003060.4:c.902C>A