Allele Registry

Canonical Allele Identifier: PA2825832475

Gene: CNST HGNC NCBI

ClinVar RCV:

RCV004112001

ClinVar Variation:

2252523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001132931.1:p.Glu313Gly	CA40581914 NM_001139459.2:c.938A>G