Canonical Allele Identifier: PA2579792696
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr53Pro
CA410602327
NM_000071.3:c.157A>C
CA2579803654
NM_000071.3:c.157_159delinsCCA
CA2579803656
NM_000071.3:c.157_159delinsCCT