Canonical Allele Identifier: PA2826132962
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 92423
ClinVar RCV Id: RCV000078105 RCV000169310 RCV001280568 RCV002228199 RCV003905038
ClinVar Variation Id: 419185
ClinVar RCV Id: RCV000487415 RCV002230902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Arg336Cys
CA274154
NM_001178008.3:c.1006C>T
CA16621014
NM_001178008.3:c.1005_1006delinsTT
CA2579812126
NM_001178008.3:c.1006_1008delinsTGT