Canonical Allele Identifier: PA102335
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4094
ClinVar RCV Id: RCV000023570 RCV000055761 RCV000169017 RCV003234891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Gly678Val
CA259844
NM_000112.4:c.2033G>T