Allele Registry

Canonical Allele Identifier: PA658812989

Gene: WFS1 HGNC NCBI

ClinVar RCV:

RCV000615392

RCV003128249

ClinVar Variation:

517479

HGVS (amino-acid)	Matching Registered Transcripts
NP_005996.2:p.Phe810Leu	CA356178561 NM_006005.3:c.2428T>C CA356178566 NM_006005.3:c.2430C>A CA356178567 NM_006005.3:c.2430C>G