Canonical Allele Identifier: PA2828733031
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1162919
ClinVar RCV Id: RCV001507556 RCV001882543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Gly37Arg
CA1600487
NM_001377959.1:c.109G>C
CA346601372
NM_001377959.1:c.109G>A