Allele Registry

Canonical Allele Identifier: PA342669

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000506707

RCV003507248

ClinVar Variation:

25408

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Leu363Pro	CA342668 NM_003060.4:c.1088T>C