Allele Registry

Canonical Allele Identifier: PA108213

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022302

RCV000414281

RCV000506183

ClinVar Variation:

25355

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Asn32Ser	CA342615 NM_003060.4:c.95A>G