Canonical Allele Identifier: PA2579794325
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gly11Leu
CA2579810095
NM_000071.3:c.31_32delinsCT
CA2579810096
NM_000071.3:c.31_32delinsTT