Canonical Allele Identifier: PA2828732993
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2132633
ClinVar RCV Id: RCV003063839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Gly6Glu
CA1600453
NM_001377959.1:c.17G>A