Allele Registry

Canonical Allele Identifier: PA093420

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000012995

RCV003556006

ClinVar Variation:

12211

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Gly96Val	CA121957 NM_000490.5:c.287G>T