Canonical Allele Identifier: PA645477544
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94366
ClinVar RCV Id: RCV000080334 RCV003236666 RCV003460754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Ser321Pro
CA222222
NM_001130987.2:c.961T>C