Canonical Allele Identifier: PA2826132681
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 197625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Arg125Gln
CA275291
NM_001178008.3:c.374G>A