Canonical Allele Identifier: PA645476986
Gene: DYSF HGNC NCBI

Linked Data


Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_001124459.1:p.Val69Leu
NM_001130987.2:c.205G>C

NM_001130987.2:c.205G>T