Canonical Allele Identifier: PA2579793933
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro88Leu
CA410602094
NM_000071.3:c.263C>T
CA2579805412
NM_000071.3:c.263_264delinsTG
CA2579805414
NM_000071.3:c.262_264delinsTTG