Canonical Allele Identifier: PA658825279
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 550585
ClinVar RCV Id: RCV000665365
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.His641Arg
CA361709384
NM_000112.4:c.1922A>G