Canonical Allele Identifier: PA645415108
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 352031
ClinVar RCV Id: RCV000281557 RCV000336484 RCV000330490 RCV000372485 RCV000376030 RCV001439481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Tyr710Cys
CA3505558
NM_000112.4:c.2129A>G