Canonical Allele Identifier: PA2826111462
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309316
ClinVar RCV Id: RCV000292543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167599.1:p.Thr216Ile
CA10633087
NM_001174128.2:c.647C>T