Allele Registry

Canonical Allele Identifier: PA2829927149

Gene: CPVL HGNC NCBI

ClinVar Allele:

2238207

ClinVar RCV:

RCV004113299

ClinVar Variation:

2250085

HGVS (amino-acid)	Matching Registered Transcripts
NP_061902.2:p.Gly3Asp	CA367241143 NM_019029.3:c.8G>A