Canonical Allele Identifier: PA2828125149
Gene: SPAST HGNC NCBI
ClinVar RCV:
RCV000644886
ClinVar Variation:
536436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Phe335Ser
CA346501201
NM_001363875.2:c.1004T>C