Canonical Allele Identifier: PA2829468894
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471318
ClinVar RCV Id: RCV000534201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Asp1855Val
CA347223572
NM_003494.4:c.5564A>T