Canonical Allele Identifier: PA2828733498
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 409032
ClinVar RCV Id: RCV000468513 RCV003972759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ala463Thr
CA16610831
NM_001377959.1:c.1387G>A