Allele Registry

Canonical Allele Identifier: PA2825832498

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004176071

ClinVar Variation:

2337314

HGVS (amino-acid)	Matching Registered Transcripts
NP_001132931.1:p.Asn541Ile	CA345515513 NM_001139459.2:c.1622A>T