Canonical Allele Identifier: PA2829789216
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2055101
ClinVar RCV Id: RCV002933161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro4Arg
CA1600449
NM_014946.4:c.11C>G