Canonical Allele Identifier: PA645408148
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 316108
ClinVar RCV Id: RCV000318542 RCV001529614 RCV002402029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Leu520Phe
CA7535527
NM_025137.4:c.1558C>T