Canonical Allele Identifier: PA2579795609
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His17Tyr
CA410602547
NM_000071.3:c.49C>T
CA2579808848
NM_000071.3:c.49_51delinsTAT