Canonical Allele Identifier: PA2828733309
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448439
ClinVar RCV Id: RCV000644904 RCV002473041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg340Ser
CA346501226
NM_001377959.1:c.1020A>C
CA346501227
NM_001377959.1:c.1020A>T