Allele Registry

Canonical Allele Identifier: PA916024763

Gene: CBS HGNC NCBI

ClinVar Variation Id: 121

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308001.1:p.Gly34Arg	CA113883 NM_001321072.1:c.100G>A CA410601731 NM_001321072.1:c.100G>C CA2579809693 NM_001321072.1:c.100_102delinsAGA