Canonical Allele Identifier: PA645477697
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282423
ClinVar RCV Id: RCV000340111 RCV001086001 RCV001820813 RCV001835749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Ala1346Val
CA1706844
NM_001130987.2:c.4037C>T