Allele Registry

Canonical Allele Identifier: PA2741818484

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV003557915

ClinVar Variation:

2742268

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Glu113Lys	CA9739425 NM_000490.5:c.337G>A