Canonical Allele Identifier: PA2826132740
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 580466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171479.1:p.Cys165Gly
CA410601405
NM_001178008.3:c.493T>G
CA2579810982
NM_001178008.3:c.493_495delinsGGG