Canonical Allele Identifier: PA2830310996
Gene: SLC22A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163314
ClinVar RCV Id: RCV004448697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694857.1:p.Gly373Arg
CA4083978
NM_153187.2:c.1117G>A
CA366328333
NM_153187.2:c.1117G>C