Canonical Allele Identifier: PA2827070245
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 944779
ClinVar RCV Id: RCV002241213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308001.1:p.Cys139Tyr
CA410600436
NM_001321072.1:c.416G>A