Canonical Allele Identifier: PA2828118659
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1303472
ClinVar RCV Id: RCV001762930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Lys10Arg
CA346601224
NM_001363823.2:c.29A>G