Canonical Allele Identifier: PA2579798359
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln298Arg
CA410600061
NM_000071.3:c.893A>G
CA2579810742
NM_000071.3:c.893_894delinsGT
CA2579810743
NM_000071.3:c.892_893delinsAG