Canonical Allele Identifier: PA2828733493
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 417628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asp461His
CA16616713
NM_001377959.1:c.1381G>C