Canonical Allele Identifier: PA334276
Gene: SPAST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Thr389Ala
CA334274
NM_014946.4:c.1165A>G