Canonical Allele Identifier: PA645415107
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284376
ClinVar RCV Id: RCV000324346 RCV000956326 RCV001271508 RCV001707611
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Asn696Ser
CA3505551
NM_000112.4:c.2087A>G