Canonical Allele Identifier: PA2579792168
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His501Gly
CA2579809153
NM_000071.3:c.1501_1503delinsGGG
CA2579809155
NM_000071.3:c.1501_1503delinsGGT