Canonical Allele Identifier: PA2579801108
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Leu426Arg
CA410397258
NM_000071.3:c.1277T>G
CA2579807315
NM_000071.3:c.1277_1278delinsGT