Canonical Allele Identifier: PA2826132752
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1922799
ClinVar RCV Id: RCV002634443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Glu176Gln
CA410601281
NM_001178008.3:c.526G>C