Canonical Allele Identifier: PA2828125227
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 586659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Val383Ala
CA346501824
NM_001363875.2:c.1148T>C