Canonical Allele Identifier: PA2829469166
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285133
ClinVar RCV Id: RCV000304230 RCV000811495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Arg2019Lys
CA10605008
NM_003494.4:c.6056G>A