Canonical Allele Identifier: PA2825768539
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 381677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Pro1988Ser
CA16604254
NM_001130985.2:c.5962C>T