Canonical Allele Identifier: PA2825750452
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Asn1365Lys
CA1706915
NM_001130977.2:c.4095C>A
CA347228802
NM_001130977.2:c.4095C>G