Canonical Allele Identifier: PA2579793955
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Met89Ile
CA321100365
NM_000071.3:c.267G>T
CA410602087
NM_000071.3:c.267G>C
CA410602088
NM_000071.3:c.267G>A