Canonical Allele Identifier: PA2579801299
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ile435Val
CA410397116
NM_000071.3:c.1303A>G
CA2579808098
NM_000071.3:c.1303_1305delinsGTA
CA2579808099
NM_000071.3:c.1303_1305delinsGTT
CA2579808100
NM_000071.3:c.1303_1305delinsGTG