Canonical Allele Identifier: PA216027
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64385
ClinVar RCV Id: RCV000054572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Thr666Ala
CA216025
NM_000112.4:c.1996A>G