Canonical Allele Identifier: PA2579796667
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His218Tyr
CA410600781
NM_000071.3:c.652C>T
CA2579808796
NM_000071.3:c.652_654delinsTAT