Canonical Allele Identifier: PA147768
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94343
ClinVar RCV Id: RCV000080309 RCV000373692 RCV000316737 RCV000546064 RCV001273966 RCV001795107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Leu189Val
CA147767
NM_003494.4:c.565C>G