Canonical Allele Identifier: PA2579801111
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Leu426Phe
CA410397267
NM_000071.3:c.1276C>T
CA2579807305
NM_000071.3:c.1276_1278delinsTTT