Canonical Allele Identifier: PA102271
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 55980
ClinVar RCV Id: RCV000049389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Tyr520Cys
CA144065
NM_000111.3:c.1559A>G