Canonical Allele Identifier: PA2826132631
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Pro88Ser
CA410602097
NM_001178008.3:c.262C>T
CA2579805409
NM_001178008.3:c.262_264delinsTCG
CA3273285688
NM_001178008.3:c.262_264delinsTCC
CA3273285703
NM_001178008.3:c.262_264delinsTCA
CA3273285709
NM_001178008.3:c.262_264delinsAGC
CA3273285802
NM_001178008.3:c.262_263delinsAG