Canonical Allele Identifier: PA645408122
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 406529
ClinVar RCV Id: RCV000460702 RCV000713418 RCV001252106 RCV002374763 RCV003942477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ser132Asn
CA7535855
NM_025137.4:c.395G>A