Canonical Allele Identifier: PA2828119171
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 417628
ClinVar RCV Id: RCV000476656 RCV001848846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Asp492His
CA16616713
NM_001363823.2:c.1474G>C