Canonical Allele Identifier: PA216021
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64383
ClinVar RCV Id: RCV000054570 RCV001069051 RCV001271550 RCV004018969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Arg58Cys
CA216019
NM_000112.4:c.172C>T