Canonical Allele Identifier: PA2828118805
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2436273
ClinVar RCV Id: RCV003138610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ile133Val
CA346602476
NM_001363823.2:c.397A>G