Canonical Allele Identifier: PA2579801279
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr434Ala
CA410397137
NM_000071.3:c.1300A>G
CA2579803808
NM_000071.3:c.1300_1302delinsGCT