Canonical Allele Identifier: PA2828118708
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5672
ClinVar RCV Id: RCV000006026 RCV000584902 RCV000845266 RCV001847588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Pro45Gln
CA117671
NM_001363823.2:c.134C>A