Canonical Allele Identifier: PA1139667989
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 903770
ClinVar RCV Id: RCV001151297 RCV001156742 RCV001156743 RCV001156744 RCV001156741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Asn281His
CA361706402
NM_000112.4:c.841A>C