Canonical Allele Identifier: PA645391698
Gene: SLC26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 242376
ClinVar RCV Id: RCV000234845 RCV002487094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_602297.1:p.Ala56Thr
CA2801756
NM_134425.4:c.166G>A