Canonical Allele Identifier: PA110973
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281067
ClinVar RCV Id: RCV000379326 RCV001244501
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Gly426Arg
CA10603801
NM_003494.4:c.1276G>A
CA347215045
NM_003494.4:c.1276G>C