Canonical Allele Identifier: PA2825767489
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471296
ClinVar RCV Id: RCV000551403 RCV001272824 RCV003144341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Pro1047Ala
CA347216998
NM_001130985.2:c.3139C>G