Canonical Allele Identifier: PA2579798315
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 897572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr296Arg
CA321091411
NM_000071.3:c.887C>G
CA2579804124
NM_000071.3:c.886_887delinsCG
CA2579804125
NM_000071.3:c.886_888delinsCGT