Allele Registry

Canonical Allele Identifier: PA121976

Gene: AVP HGNC NCBI

ClinVar Allele:

27258

ClinVar RCV:

RCV000013003

ClinVar Variation:

12219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Pro7Leu	CA121974 NM_000490.5:c.20C>T