Canonical Allele Identifier: PA2825757778
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_001124452.1:p.Gly1859Asp
CA347223179
NM_001130980.2:c.5576G>A