Canonical Allele Identifier: PA2579800775
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Trp410Cys
CA410397441
NM_000071.3:c.1230G>T
CA410397442
NM_000071.3:c.1230G>C