Canonical Allele Identifier: PA2830441217
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 989179
ClinVar RCV Id: RCV001391583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Arg456Gly
CA346502481
NM_199436.2:c.1366A>G