Canonical Allele Identifier: PA2830310992
Gene: SLC22A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163313
ClinVar RCV Id: RCV004448696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694857.1:p.Ser358Cys
CA4083970
NM_153187.2:c.1073C>G