Canonical Allele Identifier: PA099719
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_653186.2:p.Leu418Arg
CA116316
NM_144585.4:c.1253T>G