Canonical Allele Identifier: PA102306
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4093
ClinVar RCV Id: RCV000023569 RCV000055757 RCV001851641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Asn425Asp
CA259842
NM_000112.4:c.1273A>G