Canonical Allele Identifier: PA2828118691
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 409029
ClinVar RCV Id: RCV000464226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro38Arg
CA16610961
NM_001363823.2:c.113C>G