Canonical Allele Identifier: PA2826132630
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2711040
ClinVar RCV Id: RCV003496394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Pro88Arg
CA410602095
NM_001178008.3:c.263C>G