Canonical Allele Identifier: PA202203
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65560
ClinVar RCV Id: RCV000055762 RCV000176981 RCV000363939 RCV000334149 RCV000388712 RCV000269354 RCV001513704 RCV000588132 RCV002277137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Thr689Ser
CA202201
NM_000112.4:c.2065A>T
CA361709733
NM_000112.4:c.2066C>G