Canonical Allele Identifier: PA333998
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 188083
ClinVar RCV Id: RCV000167918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly546Glu
CA333996
NM_014946.4:c.1637G>A