Canonical Allele Identifier: PA2830441095
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5676
ClinVar RCV Id: RCV000006030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ser413Arg
CA253570
NM_199436.2:c.1239C>A
CA346502182
NM_199436.2:c.1237A>C
CA346502188
NM_199436.2:c.1239C>G