Canonical Allele Identifier: PA2825210665
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309316
ClinVar RCV Id: RCV000292543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000608.1:p.Thr216Ile
CA10633087
NM_000617.3:c.647C>T