Canonical Allele Identifier: PA2828118804
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344064
ClinVar RCV Id: RCV001848167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ala130_Leu131insArg
CA2573051929
NM_001363823.2:c.391_392insGGT