Canonical Allele Identifier: PA2828118718
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 898888
ClinVar RCV Id: RCV001143041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Phe53Leu
CA346601506
NM_001363823.2:c.157T>C
CA346601515
NM_001363823.2:c.159C>G
CA346601516
NM_001363823.2:c.159C>A