Canonical Allele Identifier: PA2826132639
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 471361
ClinVar RCV Id: RCV000557426 RCV002232085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Ile95Thr
CA410602047
NM_001178008.3:c.284T>C