Canonical Allele Identifier: PA2826132832
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 859601
ClinVar RCV Id: RCV002240523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Tyr233Cys
CA410600566
NM_001178008.3:c.698A>G
CA916082480
NM_001178008.3:c.698_699delinsGT