Canonical Allele Identifier: PA2579801116
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Leu426Tyr
CA2579807295
NM_000071.3:c.1276_1278delinsTAT
CA2579807296
NM_000071.3:c.1276_1277delinsTA