Canonical Allele Identifier: PA2826133709
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 500050
ClinVar RCV Id: RCV000596015 RCV002315894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Arg389Thr
CA410397816
NM_001178009.3:c.1166G>C