Canonical Allele Identifier: PA2579797043
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr236Asn
CA410600533
NM_000071.3:c.707C>A
CA2579804236
NM_000071.3:c.707_708delinsAT