Canonical Allele Identifier: PA102319
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Cys653Ser
CA252996
NM_000112.4:c.1957T>A
CA361709509
NM_000112.4:c.1958G>C