Canonical Allele Identifier: PA645395805
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393390
ClinVar RCV Id: RCV000445427 RCV001851112 RCV003128192
ClinVar Variation Id: 1513489
ClinVar RCV Id: RCV002026196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Met632Ile
CA16609253
NM_006005.3:c.1896G>T
CA356177057
NM_006005.3:c.1896G>A
CA356177058
NM_006005.3:c.1896G>C