Allele Registry

Canonical Allele Identifier: PA916024783

Gene: CBS HGNC NCBI

ClinVar RCV:

RCV000497733

ClinVar Variation:

431934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308001.1:p.Thr86Lys	CA410601079 NM_001321072.1:c.257C>A