Canonical Allele Identifier: PA2828119187
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 240950
ClinVar RCV Id: RCV000230990 RCV000713467 RCV000623007 RCV001814125 RCV003422150 RCV001847990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg498His
CA10581969
NM_001363823.2:c.1493G>A