Canonical Allele Identifier: PA645415042
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290033
ClinVar RCV Id: RCV000390686 RCV000705851 RCV001155190 RCV001155191 RCV001155192 RCV001156841 RCV002278323 RCV001156842
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Ala361Thr
CA3505383
NM_000112.4:c.1081G>A