Canonical Allele Identifier: PA2580274199
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1707680
ClinVar RCV Id: RCV002286659 RCV003269159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Asn64Ile
CA3403807
NM_003060.4:c.191A>T