Canonical Allele Identifier: PA2826133330
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1524772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Lys108Arg
CA410601950
NM_001178009.3:c.323A>G
CA2579807291
NM_001178009.3:c.322_323delinsCG