Allele Registry

Canonical Allele Identifier: PA916024744

Gene: CBS HGNC NCBI

ClinVar Allele:

422364

ClinVar RCV:

RCV000493781

RCV002231627

ClinVar Variation:

429655

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308001.1:p.Ala9Thr	CA321097898 NM_001321072.1:c.25G>A CA2579813314 NM_001321072.1:c.25_27delinsACT