Canonical Allele Identifier: PA2826133411
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1481680
ClinVar RCV Id: RCV002024992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Ala158Val
CA410601473
NM_001178009.3:c.473C>T
CA2579813165
NM_001178009.3:c.473_474delinsTC