Canonical Allele Identifier: PA2580466703
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039587
ClinVar RCV Id: RCV002907919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Gln139Glu
CA392238118
NM_025137.4:c.415C>G