Canonical Allele Identifier: PA2825191946
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 3132419
ClinVar RCV Id: RCV004421347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Gly140Arg
CA310942915
NM_000490.5:c.418G>A
CA408061253
NM_000490.5:c.418G>C