Canonical Allele Identifier: PA2825759105
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538645
ClinVar RCV Id: RCV000648017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Pro1037Gln
CA347216942
NM_001130981.2:c.3110C>A