Canonical Allele Identifier: PA658806824
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538645
ClinVar RCV Id: RCV000648017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Pro1038Gln
CA347216942
NM_001130987.2:c.3113C>A