Canonical Allele Identifier: PA2579795660
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Glu171Asp
CA410601330
NM_000071.3:c.513G>T
CA410601332
NM_000071.3:c.513G>C