ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916055798
Gene: SPG11
HGNC
NCBI
Linked Data
ClinVar Variation Id:
641830
ClinVar RCV Id:
RCV000795161
RCV002343661
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_079413.3:p.Arg1821Lys
CA7534403
NM_025137.4:c.5462G>A