Canonical Allele Identifier: PA2826924133
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 451559
ClinVar RCV Id: RCV000518895 RCV001853661 RCV002226467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Gly74Asp
CA127196443
NM_001308122.2:c.221G>A