Allele Registry

Canonical Allele Identifier: PA108436

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022372

RCV000519322

RCV000622549

RCV002226446

ClinVar Variation:

25416

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Thr440Met	CA342675 NM_003060.4:c.1319C>T