Allele Registry

Canonical Allele Identifier: PA2580524688

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004130973

ClinVar Variation:

2276875

HGVS (amino-acid)	Matching Registered Transcripts
NP_689822.2:p.Gly319Val	CA1490122 NM_152609.3:c.956G>T