Canonical Allele Identifier: PA2579798312
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr296Ala
CA410600074
NM_000071.3:c.886A>G
CA2579804126
NM_000071.3:c.886_888delinsGCT
CA2579804127
NM_000071.3:c.886_888delinsGCA
CA2579804128
NM_000071.3:c.886_888delinsGCC