Canonical Allele Identifier: PA658675013
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe524Leu
CA356176020
NM_006005.3:c.1570T>C
CA356176028
NM_006005.3:c.1572C>A
CA356176030
NM_006005.3:c.1572C>G