Canonical Allele Identifier: PA2828125334
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2816402
ClinVar RCV Id: RCV003634715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Asn454Lys
CA346502479
NM_001363875.2:c.1362T>A
CA346502480
NM_001363875.2:c.1362T>G