Canonical Allele Identifier: PA2828125353
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536434
ClinVar RCV Id: RCV000644884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Arg465Ser
CA346502816
NM_001363875.2:c.1395G>C
CA346502817
NM_001363875.2:c.1395G>T