Canonical Allele Identifier: PA2825210683
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2297722
ClinVar RCV Id: RCV002860600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000608.1:p.Glu399Lys
CA384843394
NM_000617.3:c.1195G>A