Canonical Allele Identifier: PA2825763420
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 864337
ClinVar RCV Id: RCV001071496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Phe1381Ser
CA347228816
NM_001130983.2:c.4142T>C