Canonical Allele Identifier: PA2828125301
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344051
ClinVar RCV Id: RCV001848154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Thr430Asn
CA346502309
NM_001363875.2:c.1289C>A