Allele Registry

Canonical Allele Identifier: PA342639

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022330

RCV001564243

ClinVar Variation:

38276

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Asn210Ser	CA342638 NM_003060.4:c.629A>G