Canonical Allele Identifier: PA2828119270
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 212290
ClinVar RCV Id: RCV000193599 RCV000509114 RCV000658865 RCV001640291 RCV001391562 RCV001847874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Asn578His
CA207191
NM_001363823.2:c.1732A>C