Canonical Allele Identifier: PA2830440998
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 586656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ala376Val
CA346501472
NM_199436.2:c.1127C>T