Canonical Allele Identifier: PA2825762399
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Ala426Val
CA1705708
NM_001130983.2:c.1277C>T