Canonical Allele Identifier: PA2825767527
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2441152
ClinVar RCV Id: RCV003146981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Gln1070Lys
CA347217130
NM_001130985.2:c.3208C>A