Canonical Allele Identifier: PA2579798273
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asn294Asp
CA410600090
NM_000071.3:c.880A>G
CA2579811802
NM_000071.3:c.880_882delinsGAT