Canonical Allele Identifier: PA108187
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460399
ClinVar RCV Id: RCV000528265 RCV000786403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Arg488Cys
CA3404179
NM_003060.4:c.1462C>T