Canonical Allele Identifier: PA2828119262
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344056
ClinVar RCV Id: RCV001848159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Glu562_Leu563insThrLysThr
CA2573051940
NM_001363823.2:c.1686_1687insACTAAAACC