Canonical Allele Identifier: PA2579798274
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asn294Thr
CA410600086
NM_000071.3:c.881A>C
CA2579811674
NM_000071.3:c.881_882delinsCT
CA2579811783
NM_000071.3:c.881_882delinsCA