Canonical Allele Identifier: PA2828124926
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1061785
ClinVar RCV Id: RCV001371432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Leu66Phe
CA346601656
NM_001363875.2:c.198G>C
CA346601657
NM_001363875.2:c.198G>T