Canonical Allele Identifier: PA2573162949
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462113
ClinVar RCV Id: RCV001954185
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Leu587Phe
CA361708718
NM_000112.4:c.1759C>T