Canonical Allele Identifier: PA2828118692
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 897737
ClinVar RCV Id: RCV001141199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro38Leu
CA346601380
NM_001363823.2:c.113C>T