Allele Registry

Canonical Allele Identifier: PA093468

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000013000

RCV002513002

ClinVar Variation:

12216

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Ser87Phe	CA121968 NM_000490.5:c.260C>T