Canonical Allele Identifier: PA2828119018
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 430448
ClinVar RCV Id: RCV000494283 RCV001364718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Met389Ile
CA346501341
NM_001363823.2:c.1167G>A
CA346501342
NM_001363823.2:c.1167G>T
CA346501343
NM_001363823.2:c.1167G>C