Canonical Allele Identifier: PA2825767890
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1932275
ClinVar RCV Id: RCV002649399
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Asn1391Lys
CA49779104
NM_001130985.2:c.4173C>A
CA347228694
NM_001130985.2:c.4173C>G