Canonical Allele Identifier: PA2579795980
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ser19Thr
CA410602539
NM_000071.3:c.55T>A
CA2579804644
NM_000071.3:c.55_57delinsACG