Canonical Allele Identifier: PA2579794421
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Phe111Gly
CA2579806261
NM_000071.3:c.331_333delinsGGT
CA2579806262
NM_000071.3:c.331_333delinsGGG