Canonical Allele Identifier: PA2825693393
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282209
ClinVar RCV Id: RCV000300999 RCV000358093 RCV000711546 RCV001084088 RCV001449924 RCV001276725 RCV001820812
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Met452Val
CA1705737
NM_001130455.2:c.1354A>G