ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2825757397
Gene: DYSF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
285356
ClinVar RCV Id:
RCV000530924
RCV000664797
RCV000725642
RCV003235177
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001124452.1:p.Tyr1511His
CA1707060
NM_001130980.2:c.4531T>C