Canonical Allele Identifier: PA2826133410
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 263924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Ala157Thr
CA10587952
NM_001178009.3:c.469G>A
CA2579813179
NM_001178009.3:c.469_471delinsACC