Canonical Allele Identifier: PA2829465940
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 286920
ClinVar RCV Id: RCV000342489 RCV001273965 RCV000793369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Gly178Arg
CA1705397
NM_003494.4:c.532G>A
CA347207062
NM_003494.4:c.532G>C