Canonical Allele Identifier: PA136335
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45435
ClinVar RCV Id: RCV000038639 RCV000766857 RCV002509035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala48Val
CA136334
NM_006005.3:c.143C>T