Canonical Allele Identifier: PA2579795639
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro170Ala
CA410601350
NM_000071.3:c.508C>G
CA2579805886
NM_000071.3:c.508_510delinsGCT