Canonical Allele Identifier: PA2828732990
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2055101
ClinVar RCV Id: RCV002933161
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Pro4Arg
CA1600449
NM_001377959.1:c.11C>G