Canonical Allele Identifier: PA2829467255
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 661790
ClinVar RCV Id: RCV000819285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.His1037Tyr
CA1706445
NM_003494.4:c.3109C>T