Canonical Allele Identifier: PA2579797679
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg266Thr
CA410600278
NM_000071.3:c.797G>C
CA2579813874
NM_000071.3:c.797_798delinsCC