Canonical Allele Identifier: PA2826133300
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 188988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Pro78Arg
CA274218
NM_001178009.3:c.233C>G
CA2579804795
NM_001178009.3:c.233_234delinsGG