Canonical Allele Identifier: PA2826132759
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 340088
ClinVar RCV Id: RCV000279590 RCV002348095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Val178Met
CA10650559
NM_001178008.3:c.532G>A