Canonical Allele Identifier: PA2828733060
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 898888
ClinVar RCV Id: RCV001143041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Phe53Leu
CA346601506
NM_001377959.1:c.157T>C
CA346601515
NM_001377959.1:c.159C>G
CA346601516
NM_001377959.1:c.159C>A