Canonical Allele Identifier: PA2828732991
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1693809
ClinVar RCV Id: RCV002261678 RCV003774805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Pro4Ser
CA45201382
NM_001377959.1:c.10C>T