Canonical Allele Identifier: PA2828125188
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 488605
ClinVar RCV Id: RCV000578366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Met357Lys
CA346501338
NM_001363875.2:c.1070T>A