Canonical Allele Identifier: PA2830263280
Gene: SLC26A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 50910
ClinVar RCV Id: RCV000043625 RCV002247429 RCV002513638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_619732.2:p.Glu707Lys
CA143849
NM_138718.3:c.2119G>A