Canonical Allele Identifier: PA2579797031
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_000062.1:p.Thr236Ser
NM_000071.3:c.706A>T

NM_000071.3:c.706_708delinsTCG

NM_000071.3:c.706_708delinsTCT

NM_000071.3:c.707C>G