Canonical Allele Identifier: PA2499228561
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040294
ClinVar RCV Id: RCV001343906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Pro606Thr
CA3505498
NM_000112.4:c.1816C>A