Canonical Allele Identifier: PA2828118979
Gene: SPAST HGNC NCBI
ClinVar RCV:
RCV000644886
ClinVar Variation:
536436
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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