Canonical Allele Identifier: PA2579798322
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr296Leu
CA2579804111
NM_000071.3:c.886_887delinsCT
CA2579804112
NM_000071.3:c.886_887delinsTT
CA2579804487
NM_000071.3:c.886_888delinsCTT
CA2579813425
NM_000071.3:c.886_888delinsTTA