Canonical Allele Identifier: PA2826133424
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Val168Met
CA113895
NM_001178009.3:c.502G>A