Canonical Allele Identifier: PA658812979
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 517360
ClinVar RCV Id: RCV000616575 RCV001092549 RCV003148806 RCV004533263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Asp797Asn
CA356178487
NM_006005.3:c.2389G>A