Allele Registry

Canonical Allele Identifier: PA342619

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022304

RCV000595593

ClinVar Variation:

25357

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Pro46Leu	CA342618 NM_003060.4:c.137C>T