Canonical Allele Identifier: PA110924
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_003485.1:p.Gly1842Asp
CA347223179
NM_003494.4:c.5525G>A