Canonical Allele Identifier: PA916024391
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307227.1:p.Asn228Ser
CA410600619
NM_001320298.2:c.683A>G
CA2579811810
NM_001320298.2:c.683_684delinsGT
CA2579811811
NM_001320298.2:c.682_684delinsTCT