Allele Registry

Canonical Allele Identifier: PA093359

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000012997

ClinVar Variation:

12213

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Gly54Val	CA121961 NM_000490.5:c.161G>T