Canonical Allele Identifier: PA2829465988
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_003485.1:p.Thr208Ala
CA1705427
NM_003494.4:c.622A>G