Canonical Allele Identifier: PA645477715
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336971
ClinVar RCV Id: RCV000313317 RCV000370350 RCV000517870 RCV000727268 RCV001274832 RCV001083961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Pro1418Ala
CA1706942
NM_001130987.2:c.4252C>G