Canonical Allele Identifier: PA2825761829
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 381677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Pro2002Ser
CA16604254
NM_001130982.2:c.6004C>T