Canonical Allele Identifier: PA2825747472
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 195749
ClinVar RCV Id: RCV000176395 RCV000765697 RCV001085145 RCV001271790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Gly747Ser
CA242326
NM_001130976.2:c.2239G>A