Canonical Allele Identifier: PA202206
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 196209
ClinVar RCV Id: RCV000176982 RCV000271433 RCV000320835 RCV000265444 RCV000360315 RCV000589115 RCV000384666 RCV002277383 RCV001522246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Ile574Thr
CA202204
NM_000112.4:c.1721T>C