Canonical Allele Identifier: PA2825748836
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 381677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Pro1956Ser
CA16604254
NM_001130976.2:c.5866C>T