Canonical Allele Identifier: PA2826132819
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Ala226Thr
CA16042003
NM_001178008.3:c.676G>A
CA3273290989
NM_001178008.3:c.676_678delinsACA
CA3273290991
NM_001178008.3:c.676_678delinsACG
CA3273290992
NM_001178008.3:c.676_678delinsACT