Canonical Allele Identifier: PA2825919971
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143131
ClinVar RCV Id: RCV000132655 RCV001155662 RCV001155663 RCV001195409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val412Leu
CA232842
NM_001145853.1:c.1234G>C