Canonical Allele Identifier: PA108399
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 281066
ClinVar RCV Id: RCV000275675 RCV000635344 RCV002226461 RCV002261028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser362Leu
CA10603800
NM_003060.4:c.1085C>T