Canonical Allele Identifier: PA645476988
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val70Gly
CA10604804
NM_001130987.2:c.209T>G