Canonical Allele Identifier: PA216454
Gene: SLC26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 64585
ClinVar RCV Id: RCV000054772 RCV002477180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071325.2:p.Thr562Met
CA216453
NM_022042.4:c.1685C>T