Canonical Allele Identifier: PA116651
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4099
ClinVar RCV Id: RCV000004314 RCV000004315 RCV002512749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Thr512Lys
CA116649
NM_000112.4:c.1535C>A