Canonical Allele Identifier: PA2579801451
Gene: CBS HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gly442Val
CA410397005
NM_000071.3:c.1325G>T
CA2579809227
NM_000071.3:c.1325_1326delinsTG
CA2579809228
NM_000071.3:c.1325_1326delinsTT