Canonical Allele Identifier: PA916020830
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 574461
ClinVar RCV Id: RCV000696397 RCV002226484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Leu443Val
CA3404107
NM_001308122.2:c.1327C>G