Canonical Allele Identifier: PA2829467660
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 852049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Arg1297Gly
CA1706803
NM_003494.4:c.3889A>G