Allele Registry

Canonical Allele Identifier: PA645503949

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000486229

RCV000984307

ClinVar Variation:

418493

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Pro281Leu	CA16618116 NM_003060.4:c.842C>T