Canonical Allele Identifier: PA645408148
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 316108

Amino-acid Alleles

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