Canonical Allele Identifier: PA2825767002
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Ala595Val
CA1705924
NM_001130985.2:c.1784C>T