Canonical Allele Identifier: PA234955
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 167699
ClinVar RCV Id: RCV000153965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Gly496Arg
CA234954
NM_003060.4:c.1486G>A
CA360809736
NM_003060.4:c.1486G>C