Canonical Allele Identifier: PA658661446
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 448461
ClinVar RCV Id: RCV000517770 RCV001851462 RCV002467849 RCV002467850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Asp588Gly
CA7535442
NM_025137.4:c.1763A>G