Canonical Allele Identifier: PA1139668022
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 903979
ClinVar RCV Id: RCV001151619 RCV001151620 RCV001151621 RCV001151622 RCV001151623 RCV002559461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Lys596Glu
CA361708784
NM_000112.4:c.1786A>G