Canonical Allele Identifier: PA2826924009
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25349
ClinVar RCV Id: RCV000022295 RCV000786404 RCV002298449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly12Ser
CA312960
NM_001308122.2:c.34G>A