Allele Registry

Canonical Allele Identifier: PA2828477369

Gene: CPVL HGNC NCBI

ClinVar Allele:

2238207

ClinVar RCV:

RCV004113299

ClinVar Variation:

2250085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358185.1:p.Gly3Asp	CA367241143 NM_001371256.1:c.8G>A