Canonical Allele Identifier: PA2825920183
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2151042
ClinVar RCV Id: RCV003067874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Val536Leu
CA356176219
NM_001145853.1:c.1606G>T
CA356176224
NM_001145853.1:c.1606G>C