Canonical Allele Identifier: PA2829992379
Gene: SLC26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 242374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071325.2:p.Thr185Met
CA2801632
NM_022042.4:c.554C>T