Allele Registry

Canonical Allele Identifier: PA2826132659

Gene: CBS HGNC NCBI

ClinVar Allele:

422364

ClinVar RCV:

RCV000493781

RCV002231627

ClinVar Variation:

429655

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171479.1:p.Ala114Thr	CA321097898 NM_001178008.3:c.340G>A CA2579813314 NM_001178008.3:c.340_342delinsACT