Allele Registry

Canonical Allele Identifier: PA2499232862

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV001702024

ClinVar Variation:

1285212

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Ser87Tyr	CA408061593 NM_000490.5:c.260C>A