Canonical Allele Identifier: PA2579793989
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg91Ser
CA410602075
NM_000071.3:c.273A>T
CA410602076
NM_000071.3:c.273A>C
CA2579813861
NM_000071.3:c.271_273delinsTCT
CA2579813862
NM_000071.3:c.271_272delinsTC