Canonical Allele Identifier: PA2828118990
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1502317
ClinVar RCV Id: RCV002020175
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ala372Pro
CA346501229
NM_001363823.2:c.1114G>C