Allele Registry

Canonical Allele Identifier: PA093478

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000013005

ClinVar Variation:

12221

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Tyr21His	CA121979 NM_000490.5:c.61T>C