Canonical Allele Identifier: PA208998
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 188231
ClinVar RCV Id: RCV000168174 RCV000194672 RCV000512885 RCV001847791 RCV003917574 RCV002362861
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Asn2075Ser
CA208997
NM_025137.4:c.6224A>G