Canonical Allele Identifier: PA2828125238
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1348218
ClinVar RCV Id: RCV002050789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Glu387Asp
CA346501868
NM_001363875.2:c.1161G>C
CA346501869
NM_001363875.2:c.1161G>T