Canonical Allele Identifier: PA2828118985
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 397539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Leu370Phe
CA16609412
NM_001363823.2:c.1108C>T