Canonical Allele Identifier: PA2826924020
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 6429
ClinVar RCV Id: RCV000006798 RCV000186150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly15Trp
CA312963
NM_001308122.2:c.43G>T