Canonical Allele Identifier: PA109187
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9074
ClinVar RCV Id: RCV000009642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167597.1:p.Glu399Asp
CA120092
NM_001174126.2:c.1197G>C
CA384843381
NM_001174126.2:c.1197G>T