Canonical Allele Identifier: PA2828124934
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1969356
ClinVar RCV Id: RCV002730090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Phe75Leu
CA45201396
NM_001363875.2:c.225C>A
CA346601767
NM_001363875.2:c.223T>C
CA346601783
NM_001363875.2:c.225C>G