Canonical Allele Identifier: PA111012
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288438
ClinVar RCV Id: RCV000597376 RCV000726165 RCV001214514 RCV003469244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Gly621Arg
CA10606091
NM_003494.4:c.1861G>A
CA347218631
NM_003494.4:c.1861G>C