Canonical Allele Identifier: PA108137
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25401
ClinVar RCV Id: RCV000022354 RCV000413524 RCV003258656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Arg282Gln
CA342661
NM_003060.4:c.845G>A