Canonical Allele Identifier: PA2580104019
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136342
ClinVar RCV Id: RCV003037127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Ser157Thr
CA361705059
NM_000112.4:c.469T>A