Canonical Allele Identifier: PA2825748244
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94321
ClinVar RCV Id: RCV000080287 RCV000177998 RCV000536105 RCV003460751 RCV003993797
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gly1404Asp
CA222164
NM_001130976.2:c.4211G>A