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