Canonical Allele Identifier: PA2741834221
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2885593
ClinVar RCV Id: RCV003735522
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asp1876His
CA347223076
NM_001130987.2:c.5626G>C