Canonical Allele Identifier: PA2828119180
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536434
ClinVar RCV Id: RCV000644884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg497Ser
CA346502816
NM_001363823.2:c.1491G>C
CA346502817
NM_001363823.2:c.1491G>T