Canonical Allele Identifier: PA2825754718
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282705
ClinVar RCV Id: RCV000284503 RCV000648010
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Val1150Met
CA1706555
NM_001130979.2:c.3448G>A