Canonical Allele Identifier: PA2825695769
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282408
ClinVar RCV Id: RCV000317613 RCV000754725 RCV002521880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Tyr1878His
CA1707485
NM_001130455.2:c.5632T>C