Canonical Allele Identifier: PA2579801006
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala421Thr
CA410397339
NM_000071.3:c.1261G>A
CA2579812590
NM_000071.3:c.1261_1263delinsACA
CA2579812591
NM_000071.3:c.1261_1263delinsACT
CA2579812592
NM_000071.3:c.1261_1263delinsACG