Canonical Allele Identifier: PA2825758737
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 259069
ClinVar RCV Id: RCV000251223 RCV001081560 RCV001828138 RCV000513999 RCV002519917
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Leu702Val
CA1706042
NM_001130981.2:c.2104C>G