Canonical Allele Identifier: PA2825692975
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336945
ClinVar RCV Id: RCV000284809 RCV000376994 RCV000553818 RCV000732976 RCV001276721
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Thr209Ala
CA1705427
NM_001130455.2:c.625A>G