Canonical Allele Identifier: PA2829467812
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 864337
ClinVar RCV Id: RCV001071496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Phe1380Ser
CA347228816
NM_003494.4:c.4139T>C