Canonical Allele Identifier: PA645477819
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 430739
ClinVar RCV Id: RCV000494731
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly1881Asp
CA347223179
NM_001130987.2:c.5642G>A