Canonical Allele Identifier: PA2829789227
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1303472
ClinVar RCV Id: RCV001762930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Lys10Arg
CA346601224
NM_014946.4:c.29A>G