Canonical Allele Identifier: PA2825770086
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2152669
ClinVar RCV Id: RCV003075109
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Ser1340Phe
CA347228496
NM_001130986.2:c.4019C>T