Canonical Allele Identifier: PA2579797000
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asp234Tyr
CA410600559
NM_000071.3:c.700G>T
CA2579811517
NM_000071.3:c.700_702delinsTAT