Canonical Allele Identifier: PA2826111476
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2297722
ClinVar RCV Id: RCV002860600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167599.1:p.Glu399Lys
CA384843394
NM_001174128.2:c.1195G>A