Canonical Allele Identifier: PA915974000
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281301
ClinVar RCV Id: RCV000382528 RCV000648004 RCV001272831 RCV003243035
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Asp1195Asn
CA1706621
NM_001130982.2:c.3583G>A