Canonical Allele Identifier: PA2826133541
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Gly256Val
CA410600333
NM_001178009.3:c.767G>T
CA2579809500
NM_001178009.3:c.767_768delinsTT