Canonical Allele Identifier: PA2580207949
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1922799
ClinVar RCV Id: RCV002634443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308001.1:p.Glu71Gln
CA410601281
NM_001321072.1:c.211G>C