Canonical Allele Identifier: PA2830441174
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 468565
ClinVar RCV Id: RCV000526604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Gly439Asp
CA346502364
NM_199436.2:c.1316G>A
CA2586964768
NM_199436.2:c.1316_1317delinsAC