Canonical Allele Identifier: PA2828118658
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2420948
ClinVar RCV Id: RCV003112608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Lys9Arg
CA346601216
NM_001363823.2:c.26A>G