Canonical Allele Identifier: PA2825747969
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281301
ClinVar RCV Id: RCV000382528 RCV000648004 RCV001272831 RCV003243035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Asp1149Asn
CA1706621
NM_001130976.2:c.3445G>A