Canonical Allele Identifier: PA263254
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 56015
ClinVar RCV Id: RCV000049424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Gly484Asp
CA263252
NM_000112.4:c.1451G>A