Canonical Allele Identifier: PA102291
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4089
ClinVar RCV Id: RCV000004305 RCV000004306 RCV000004307 RCV000266165 RCV000275762 RCV000624686 RCV000641290 RCV000586600 RCV000999764 RCV001030752 RCV001030753 RCV002276530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Arg279Trp
CA252990
NM_000112.4:c.835C>T