Canonical Allele Identifier: PA2825755884
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336943
ClinVar RCV Id: RCV000363042 RCV000394798 RCV001139686
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Thr124Ala
CA10613906
NM_001130980.2:c.370A>G