Canonical Allele Identifier: PA645486823
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_001167596.1:p.Thr245Ile
CA10633087
NM_001174125.2:c.734C>T