Canonical Allele Identifier: PA2826111603
Gene: SLC11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9074
ClinVar RCV Id: RCV000009642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167601.1:p.Glu395Asp
CA120092
NM_001174130.2:c.1185G>C
CA384843381
NM_001174130.2:c.1185G>T