Canonical Allele Identifier: PA2579794127
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys97Asn
CA410602031
NM_000071.3:c.291G>T
CA410602032
NM_000071.3:c.291G>C