Canonical Allele Identifier: PA2829465728
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Val69Gly
CA10604804
NM_003494.4:c.206T>G