Canonical Allele Identifier: PA2579801280
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr434Val
CA2579803794
NM_000071.3:c.1300_1302delinsGTG
CA2579803795
NM_000071.3:c.1300_1302delinsGTT