ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825753561
Gene: DYSF
HGNC
NCBI
Linked Data
ClinVar Variation Id:
288625
ClinVar RCV Id:
RCV000271058
RCV001855211
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001124451.1:p.Thr74Met
CA1705259
NM_001130979.2:c.221C>T