Allele Registry

Canonical Allele Identifier: PA093111

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000012990

RCV001701565

ClinVar Variation:

12206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Ala19Thr	CA121950 NM_000490.5:c.55G>A