Canonical Allele Identifier: PA2825920795
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2806820
ClinVar RCV Id: RCV003681974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Phe884Leu
CA356179708
NM_001145853.1:c.2650T>C
CA356179725
NM_001145853.1:c.2652C>A
CA356179728
NM_001145853.1:c.2652C>G