Canonical Allele Identifier: PA282579
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45440
ClinVar RCV Id: RCV000038644 RCV000284377 RCV000445501 RCV000374202 RCV000870649 RCV002464004
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Ala602Val
CA282578
NM_006005.3:c.1805C>T