Canonical Allele Identifier: PA2579797032
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr236Ala
CA410600537
NM_000071.3:c.706A>G
CA2579804237
NM_000071.3:c.706_708delinsGCA
CA2579804238
NM_000071.3:c.706_708delinsGCT
CA2579804240
NM_000071.3:c.706_708delinsGCG