Allele Registry

Canonical Allele Identifier: PA2826132695

Gene: CBS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

210440

533942

ClinVar RCV:

RCV000196511

RCV000469139

RCV000648115

RCV002517171

RCV002533344

ClinVar Variation:

212879

538695

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171479.1:p.Gly134Arg	CA320927 NM_001178008.3:c.400G>A CA321097659 NM_001178008.3:c.400G>C CA2579809704 NM_001178008.3:c.400_402delinsAGA