Canonical Allele Identifier: PA915973849
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538645
ClinVar RCV Id: RCV000648017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Pro1052Gln
CA347216942
NM_001130982.2:c.3155C>A