Canonical Allele Identifier: PA2825920097
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1417343
ClinVar RCV Id: RCV001938300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Thr487Ser
CA2839360
NM_001145853.1:c.1460C>G
CA356175047
NM_001145853.1:c.1459A>T