Allele Registry

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Canonical Allele Identifier: PA2828733387

Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2097662

ClinVar RCV Id: RCV003018918

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364888.1:p.Gly387Arg	CA346501849 NM_001377959.1:c.1159G>A CA346501851 NM_001377959.1:c.1159G>C