Allele Registry

Canonical Allele Identifier: PA645511161

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000506707

RCV003507248

ClinVar Variation:

25408

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Leu387Pro	CA342668 NM_001308122.2:c.1160T>C