Canonical Allele Identifier: PA2579794058
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys94Thr
CA410602056
NM_000071.3:c.281A>C
CA2579813513
NM_000071.3:c.281_282delinsCT