Canonical Allele Identifier: PA2579796972
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Tyr233Asp
CA410600569
NM_000071.3:c.697T>G
CA2579803515
NM_000071.3:c.697_699delinsGAT