Canonical Allele Identifier: PA2828118687
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1038883
ClinVar RCV Id: RCV001342255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro34Leu
CA1600484
NM_001363823.2:c.101C>T