Canonical Allele Identifier: PA2579795622
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Met169Ile
CA410601352
NM_000071.3:c.507G>T
CA410601354
NM_000071.3:c.507G>A
CA410601356
NM_000071.3:c.507G>C