Canonical Allele Identifier: PA2826111498
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309304
ClinVar RCV Id: RCV000390498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167599.1:p.Ala555Thr
CA6566428
NM_001174128.2:c.1663G>A