Allele Registry

Canonical Allele Identifier: PA2825832443

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004287037

ClinVar Variation:

2494966

HGVS (amino-acid)	Matching Registered Transcripts
NP_001132931.1:p.Leu43Pro	CA1489869 NM_001139459.2:c.128T>C