Canonical Allele Identifier: PA2579796953
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His232Leu
CA410600577
NM_000071.3:c.695A>T
CA2579808755
NM_000071.3:c.695_696delinsTT
CA2579808757
NM_000071.3:c.695_696delinsTG
CA2579808758
NM_000071.3:c.694_696delinsTTG