Allele Registry

Canonical Allele Identifier: PA093351

Gene: AVP HGNC NCBI

ClinVar Allele:

27253

ClinVar RCV:

RCV000012998

ClinVar Variation:

12214

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Gly54Arg	CA121963 NM_000490.5:c.160G>C CA408061811 NM_000490.5:c.160G>A