Canonical Allele Identifier: PA2579794999
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gly14Cys
CA410602566
NM_000071.3:c.40G>T
CA2579809654
NM_000071.3:c.40_42delinsTGT