Canonical Allele Identifier: PA2828119044
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 418502
ClinVar RCV Id: RCV000481977 RCV002525773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ala408Thr
CA16617528
NM_001363823.2:c.1222G>A