Allele Registry

Canonical Allele Identifier: PA2580115932

Gene: AVP HGNC NCBI

ClinVar Allele:

1692814

ClinVar RCV:

RCV002274670

ClinVar Variation:

1700421

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Gly88Cys	CA408061590 NM_000490.5:c.262G>T