Canonical Allele Identifier: PA2829465697
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289471
ClinVar RCV Id: RCV000536797 RCV000711545 RCV001835762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Val42Met
CA1705230
NM_003494.4:c.124G>A