Canonical Allele Identifier: PA2830441021
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2760492
ClinVar RCV Id: RCV003524742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Lys382Gln
CA346501505
NM_199436.2:c.1144A>C