Allele Registry

Canonical Allele Identifier: PA342614

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022301

RCV001549353

ClinVar Variation:

25354

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Ser28Ile	CA342613 NM_003060.4:c.83G>T