ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825755505
Gene: DYSF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2144690
ClinVar RCV Id:
RCV003071061
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001124451.1:p.Ser1867Asn
CA347223063
NM_001130979.2:c.5600G>A