Canonical Allele Identifier: PA2825771815
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 864337
ClinVar RCV Id: RCV001071496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Phe1398Ser
CA347228816
NM_001130987.2:c.4193T>C