Canonical Allele Identifier: PA2579795681
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys172Ser
CA2579806838
NM_000071.3:c.514_516delinsTCT
CA2579806839
NM_000071.3:c.515_516delinsGT
CA2579806840
NM_000071.3:c.514_515delinsTC