Canonical Allele Identifier: PA2828733452
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344051
ClinVar RCV Id: RCV001848154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Thr431Asn
CA346502309
NM_001377959.1:c.1292C>A