Canonical Allele Identifier: PA2573070332
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1310379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307227.1:p.Ala226Pro
CA321095500
NM_001320298.2:c.676G>C