Canonical Allele Identifier: PA2825694229
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538645
ClinVar RCV Id: RCV000648017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Pro1021Gln
CA347216942
NM_001130455.2:c.3062C>A