Canonical Allele Identifier: PA2579793947
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Met89Val
CA410602092
NM_000071.3:c.265A>G
CA2579806268
NM_000071.3:c.265_267delinsGTT