Canonical Allele Identifier: PA2741818487
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 2896713
ClinVar RCV Id: RCV003731069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Ala141Val
CA310942881
NM_000490.5:c.422C>T