Canonical Allele Identifier: PA2828733516
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 219575
ClinVar RCV Id: RCV000204046 RCV000585136 RCV001847923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg471Trp
CA348315
NM_001377959.1:c.1411C>T