Canonical Allele Identifier: PA2825750975
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 430739
ClinVar RCV Id: RCV000494731
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Gly1849Asp
CA347223179
NM_001130977.2:c.5546G>A