Canonical Allele Identifier: PA2828118712
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2154832
ClinVar RCV Id: RCV003069485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg48Trp
CA346601449
NM_001363823.2:c.142C>T