Canonical Allele Identifier: PA116648
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4096
ClinVar RCV Id: RCV000004311 RCV000055758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Gln454Pro
CA116646
NM_000112.4:c.1361A>C