Canonical Allele Identifier: PA2828118796
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1298799
ClinVar RCV Id: RCV001727129 RCV003771877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Phe124Leu
CA346602417
NM_001363823.2:c.370T>C
CA346602421
NM_001363823.2:c.372C>A
CA346602422
NM_001363823.2:c.372C>G