Canonical Allele Identifier: PA2828118743
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1969356
ClinVar RCV Id: RCV002730090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Phe75Leu
CA45201396
NM_001363823.2:c.225C>A
CA346601767
NM_001363823.2:c.223T>C
CA346601783
NM_001363823.2:c.225C>G