Allele Registry

Canonical Allele Identifier: PA916020755

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022330

RCV001564243

ClinVar Variation:

38276

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Asn234Ser	CA342638 NM_001308122.2:c.701A>G