Canonical Allele Identifier: PA2826111589
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_001167601.1:p.Thr212Ile
CA10633087
NM_001174130.2:c.635C>T