Canonical Allele Identifier: PA2579795816
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg18Tyr
CA2579812757
NM_000071.3:c.52_54delinsTAT
CA2579812758
NM_000071.3:c.52_53delinsTA