Canonical Allele Identifier: PA2579792101
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg498Gly
CA410395809
NM_000071.3:c.1492A>G
CA2579811879
NM_000071.3:c.1492_1494delinsGGT