Canonical Allele Identifier: PA2825667288
Gene: SLC39A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 289730
ClinVar RCV Id: RCV000399888 RCV000535171 RCV001697652 RCV002278322 RCV002278321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121697.2:p.Arg40Gln
CA5975670
NM_001128225.3:c.119G>A