Canonical Allele Identifier: PA2741923631
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2856819
ClinVar RCV Id: RCV003696600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ser617Arg
CA356176956
NM_006005.3:c.1849A>C
CA356176962
NM_006005.3:c.1851C>A
CA356176963
NM_006005.3:c.1851C>G