Canonical Allele Identifier: PA645477602
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281014
ClinVar RCV Id: RCV000274204 RCV000710126 RCV001084090 RCV001329088 RCV003920032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Met644Thr
CA1705983
NM_001130987.2:c.1931T>C