Allele Registry

Canonical Allele Identifier: PA2580524674

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004287037

ClinVar Variation:

2494966

HGVS (amino-acid)	Matching Registered Transcripts
NP_689822.2:p.Leu43Pro	CA1489869 NM_152609.3:c.128T>C