Canonical Allele Identifier: PA2825754575
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538645
ClinVar RCV Id: RCV000648017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Pro1051Gln
CA347216942
NM_001130979.2:c.3152C>A