Canonical Allele Identifier: PA263262
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 56022
ClinVar RCV Id: RCV000049431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Asp111Tyr
CA263260
NM_000112.4:c.331G>T