Canonical Allele Identifier: PA2828733021
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 964686
ClinVar RCV Id: RCV001238954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Cys28Ser
CA346601322
NM_001377959.1:c.82T>A
CA346601326
NM_001377959.1:c.83G>C