Allele Registry

Canonical Allele Identifier: PA645503972

Gene: SLC22A5 HGNC NCBI

ClinVar Allele:

414985

ClinVar RCV:

RCV000490211

RCV001276453

ClinVar Variation:

426359

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Ile348Lys	CA3404050 NM_003060.4:c.1043T>A