Allele Registry

Canonical Allele Identifier: PA093117

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000012996

ClinVar Variation:

12212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Ala19Val	CA121959 NM_000490.5:c.56C>T