Canonical Allele Identifier: PA147748
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Gly128Glu
CA147747
NM_003494.4:c.383G>A