Canonical Allele Identifier: PA2579794037
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asn93Thr
CA410602063
NM_000071.3:c.278A>C
CA2579811582
NM_000071.3:c.278_279delinsCG