Allele Registry

Canonical Allele Identifier: PA2825832489

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004232350

ClinVar Variation:

2392924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001132931.1:p.Arg441His	CA1490206 NM_001139459.2:c.1322G>A