Canonical Allele Identifier: PA110819
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6677
ClinVar RCV Id: RCV000007064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Asp625Tyr
CA253909
NM_003494.4:c.1873G>T