Canonical Allele Identifier: PA2826111359
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3162806
ClinVar RCV Id: RCV004456205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167597.1:p.Ala371Val
CA384843755
NM_001174126.2:c.1112C>T