Canonical Allele Identifier: PA2828733333
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 450255
ClinVar RCV Id: RCV000521931 RCV000528465
ClinVar Variation Id: 1454039
ClinVar RCV Id: RCV001960564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Lys356Asn
CA346501329
NM_001377959.1:c.1068G>C
CA346501330
NM_001377959.1:c.1068G>T