Canonical Allele Identifier: PA2579795690
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys172Asn
CA410601318
NM_000071.3:c.516G>T
CA410601319
NM_000071.3:c.516G>C