Allele Registry

Canonical Allele Identifier: PA093281

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000013001

RCV003407322

ClinVar Variation:

12217

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Cys92Tyr	CA121970 NM_000490.5:c.275G>A