Canonical Allele Identifier: PA2579793970
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Val90Asp
CA410602083
NM_000071.3:c.269T>A
CA2579802758
NM_000071.3:c.269_270delinsAT