Canonical Allele Identifier: PA2825760038
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 500678
ClinVar RCV Id: RCV000593308 RCV003231652
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Met1873Val
CA347223040
NM_001130981.2:c.5617A>G