Canonical Allele Identifier: PA2828118807
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1675774
ClinVar RCV Id: RCV002214143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Lys138Glu
CA346602515
NM_001363823.2:c.412A>G