Canonical Allele Identifier: PA2579800837
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg413Gly
CA410397416
NM_000071.3:c.1237C>G
CA2579811964
NM_000071.3:c.1237_1239delinsGGG