Canonical Allele Identifier: PA2579798328
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr296Pro
CA410600075
NM_000071.3:c.886A>C
CA2579804484
NM_000071.3:c.886_888delinsCCA
CA2579804485
NM_000071.3:c.886_888delinsCCT