Canonical Allele Identifier: PA2825768734
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_001124458.1:p.Asn103Ser
CA1705307
NM_001130986.2:c.308A>G