Canonical Allele Identifier: PA2580115942
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 1929919
ClinVar RCV Id: RCV002618790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Arg145Pro
CA310942870
NM_000490.5:c.434G>C