Canonical Allele Identifier: PA2825759740
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501558
ClinVar RCV Id: RCV000594913 RCV000797230
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Ala1610Thr
CA1707154
NM_001130981.2:c.4828G>A