Canonical Allele Identifier: PA2579797041
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr236Tyr
CA2579804216
NM_000071.3:c.706_708delinsTAT
CA2579804217
NM_000071.3:c.706_707delinsTA