Canonical Allele Identifier: PA2828830304
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9074
ClinVar RCV Id: RCV000009642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366376.1:p.Glu399Asp
CA120092
NM_001379447.1:c.1197G>C
CA384843381
NM_001379447.1:c.1197G>T