Canonical Allele Identifier: PA2829419321
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2073959
ClinVar RCV Id: RCV002975951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser402Cys
CA360807742
NM_003060.4:c.1205C>G