Canonical Allele Identifier: PA2825749059
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538621
ClinVar RCV Id: RCV000647984 RCV001253301
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Asn102Ser
CA1705307
NM_001130977.2:c.305A>G