Canonical Allele Identifier: PA2830441044
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2097662
ClinVar RCV Id: RCV003018918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Gly387Arg
CA346501849
NM_199436.2:c.1159G>A
CA346501851
NM_199436.2:c.1159G>C