Canonical Allele Identifier: PA2830441045
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2125906
ClinVar RCV Id: RCV003043857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Gly387Val
CA346501856
NM_199436.2:c.1160G>T