Canonical Allele Identifier: PA2825920333
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2186674
ClinVar RCV Id: RCV002606819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val620Leu
CA2839522
NM_001145853.1:c.1858G>C
CA356176979
NM_001145853.1:c.1858G>T