Canonical Allele Identifier: PA2828119074
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1723186
ClinVar RCV Id: RCV002306283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg423Ser
CA346502039
NM_001363823.2:c.1269G>C
CA346502040
NM_001363823.2:c.1269G>T