Allele Registry

Canonical Allele Identifier: PA117719

Gene: SLC22A4 HGNC NCBI

ClinVar RCV:

RCV000006106

RCV001682707

ClinVar Variation:

5750

HGVS (amino-acid)	Matching Registered Transcripts
NP_003050.2:p.Leu503Phe	CA117718 NM_003059.3:c.1507C>T