Canonical Allele Identifier: PA2825767471
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471294
ClinVar RCV Id: RCV000548061 RCV001829588
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Ile1034Met
CA1706423
NM_001130985.2:c.3102C>G