Canonical Allele Identifier: PA2741923611
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2764668
ClinVar RCV Id: RCV003572611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Thr595Ser
CA2839489
NM_006005.3:c.1784C>G
CA356176844
NM_006005.3:c.1783A>T