Canonical Allele Identifier: PA2825751149
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285133
ClinVar RCV Id: RCV000304230 RCV000811495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Arg2026Lys
CA10605008
NM_001130977.2:c.6077G>A