Canonical Allele Identifier: PA2573182991
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1503167
ClinVar RCV Id: RCV002045365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Val1398Leu
CA347228569
NM_001130982.2:c.4192G>C
CA347228570
NM_001130982.2:c.4192G>T