Canonical Allele Identifier: PA2830441142
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1298800
ClinVar RCV Id: RCV001727130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Leu429Pro
CA346502296
NM_199436.2:c.1286T>C