Canonical Allele Identifier: PA2828125272
Gene: SPAST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ser412Arg
CA253570
NM_001363875.2:c.1236C>A
CA346502182
NM_001363875.2:c.1234A>C
CA346502188
NM_001363875.2:c.1236C>G