Canonical Allele Identifier: PA2579798016
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro282Ala
CA410600159
NM_000071.3:c.844C>G
CA2579805477
NM_000071.3:c.844_846delinsGCT