Canonical Allele Identifier: PA102186
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 55985
ClinVar RCV Id: RCV000049394 RCV003556122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Ile544Asn
CA144074
NM_000111.3:c.1631T>A