Canonical Allele Identifier: PA2826144097
Gene: SLC22A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163494
ClinVar RCV Id: RCV004451354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171665.1:p.Arg168Ser
CA223623839
NM_001184736.2:c.504G>T
CA380982495
NM_001184736.2:c.504G>C