Canonical Allele Identifier: PA2826132629
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2452200
ClinVar RCV Id: RCV003172294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Thr87Ile
CA410602100
NM_001178008.3:c.260C>T
CA2579804004
NM_001178008.3:c.260_261delinsTA