Canonical Allele Identifier: PA2573162851
Gene: SLC26A3 HGNC NCBI
ClinVar RCV:
RCV002001808
ClinVar Variation:
1490634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Thr744Ile
CA368849418
NM_000111.3:c.2231C>T