Canonical Allele Identifier: PA2828118979
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536436
ClinVar RCV Id: RCV000644886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Phe367Ser
CA346501201
NM_001363823.2:c.1100T>C