Canonical Allele Identifier: PA2579798314
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr296Ser
CA410600076
NM_000071.3:c.886A>T
CA2579804109
NM_000071.3:c.887_888delinsGT
CA2579804110
NM_000071.3:c.886_888delinsTCT
CA2579804483
NM_000071.3:c.886_888delinsTCC
CA2579813403
NM_000071.3:c.886_888delinsTCA