Allele Registry

Canonical Allele Identifier: PA2580524687

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004112001

ClinVar Variation:

2252523

HGVS (amino-acid)	Matching Registered Transcripts
NP_689822.2:p.Glu313Gly	CA40581914 NM_152609.3:c.938A>G