Canonical Allele Identifier: PA2825762543
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 498346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Arg583Trp
CA1705929
NM_001130983.2:c.1747C>T