Canonical Allele Identifier: PA2579798393
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr299Pro
CA410600056
NM_000071.3:c.895A>C
CA2579804086
NM_000071.3:c.895_897delinsCCT