Canonical Allele Identifier: PA2579798376
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln298His
CA410600057
NM_000071.3:c.894G>T
CA410600058
NM_000071.3:c.894G>C