Canonical Allele Identifier: PA2579794009
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ile92Ser
CA410602069
NM_000071.3:c.275T>G
CA2579808338
NM_000071.3:c.274_276delinsTCT