Canonical Allele Identifier: PA645477586
Gene: DYSF HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001124459.1:p.Gly537Arg
NM_001130987.2:c.1609G>A

NM_001130987.2:c.1609G>C