Canonical Allele Identifier: PA2579798357
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln298Ser
CA2579810729
NM_000071.3:c.892_893delinsTC
CA2579810730
NM_000071.3:c.892_894delinsTCT
CA2579813815
NM_000071.3:c.892_894delinsAGT