Canonical Allele Identifier: PA2828124922
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1707912
ClinVar RCV Id: RCV002287073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Phe61Leu
CA346601599
NM_001363875.2:c.181T>C
CA346601609
NM_001363875.2:c.183C>A
CA346601611
NM_001363875.2:c.183C>G