Canonical Allele Identifier: PA2828124900
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 897739
ClinVar RCV Id: RCV001141201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.His46Arg
CA1600500
NM_001363875.2:c.137A>G