Canonical Allele Identifier: PA108482
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 6420
ClinVar RCV Id: RCV000006789 RCV000186136 RCV002226443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Tyr211Cys
CA312941
NM_003060.4:c.632A>G