Canonical Allele Identifier: PA2579798372
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln298Pro
CA410600060
NM_000071.3:c.893A>C
CA2579810732
NM_000071.3:c.893_894delinsCT
CA2579813816
NM_000071.3:c.893_894delinsCA