Canonical Allele Identifier: PA916020810
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_001295051.1:p.Ser386Leu
CA10603800
NM_001308122.2:c.1157C>T