Canonical Allele Identifier: PA2826554134
Gene: SLC22A12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3515
ClinVar RCV Id: RCV000003692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263255.1:p.Leu384Arg
CA116316
NM_001276326.2:c.1151T>G