Canonical Allele Identifier: PA2828118995
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 424653
ClinVar RCV Id: RCV000516040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Leu377Gln
CA346501261
NM_001363823.2:c.1130T>A