Canonical Allele Identifier: PA645415040
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 352025
ClinVar RCV Id: RCV000281048 RCV000312752 RCV000338459 RCV000390859 RCV000399511 RCV000591740 RCV000765823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Phe349Tyr
CA3505378
NM_000112.4:c.1046T>A