Canonical Allele Identifier: PA2828733368
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 963588
ClinVar RCV Id: RCV001237635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser378Arg
CA346501478
NM_001377959.1:c.1132A>C
CA346501484
NM_001377959.1:c.1134T>A
CA346501485
NM_001377959.1:c.1134T>G