Canonical Allele Identifier: PA2825920697
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2692084
ClinVar RCV Id: RCV003494281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Trp837Cys
CA356178784
NM_001145853.1:c.2511G>C
CA356178785
NM_001145853.1:c.2511G>T