Canonical Allele Identifier: PA2579799877
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln368Pro
CA410398061
NM_000071.3:c.1103A>C
CA2579810652
NM_000071.3:c.1103_1104delinsCT