Canonical Allele Identifier: PA2825920206
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179874
ClinVar RCV Id: RCV000156674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139325.1:p.Leu549Val
CA185322
NM_001145853.1:c.1645C>G