Canonical Allele Identifier: PA2826133551
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Thr262Arg
CA410600299
NM_001178009.3:c.785C>G
CA2579804154
NM_001178009.3:c.785_786delinsGA
CA2579804155
NM_001178009.3:c.784_785delinsCG
CA2579804156
NM_001178009.3:c.784_786delinsCGT