Canonical Allele Identifier: PA2579792041
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr495Pro
CA410395847
NM_000071.3:c.1483A>C
CA2579803724
NM_000071.3:c.1483_1485delinsCCT