Allele Registry

Canonical Allele Identifier: PA2825832477

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004130973

ClinVar Variation:

2276875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001132931.1:p.Gly319Val	CA1490122 NM_001139459.2:c.956G>T