Canonical Allele Identifier: PA2825746936
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290515
ClinVar RCV Id: RCV000333472 RCV000812750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gln221His
CA10606797
NM_001130976.2:c.663G>C
CA347207711
NM_001130976.2:c.663G>T