Canonical Allele Identifier: PA2828124838
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1344038
ClinVar RCV Id: RCV001848141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Pro4Ala
CA346601190
NM_001363875.2:c.10C>G