Canonical Allele Identifier: PA2828733304
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1056688
ClinVar RCV Id: RCV001365555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Gly338Trp
CA346501213
NM_001377959.1:c.1012G>T