Canonical Allele Identifier: PA2828733431
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536442
ClinVar RCV Id: RCV000644893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg418Gly
CA346502217
NM_001377959.1:c.1252A>G