Canonical Allele Identifier: PA2580103949
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1899777
ClinVar RCV Id: RCV002575649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Lys723Met
CA368849582
NM_000111.3:c.2168A>T