Canonical Allele Identifier: PA2828118655
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 3004860
ClinVar RCV Id: RCV003860963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Gly8Glu
CA346601209
NM_001363823.2:c.23G>A