Canonical Allele Identifier: PA2828124905
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 835946
ClinVar RCV Id: RCV001036951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Tyr51Cys
CA346601485
NM_001363875.2:c.152A>G