Canonical Allele Identifier: PA658807009
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 500678
ClinVar RCV Id: RCV000593308 RCV003231652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Met1874Val
CA347223040
NM_001130987.2:c.5620A>G