Canonical Allele Identifier: PA2825191942
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 3132418
ClinVar RCV Id: RCV004421346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Gly137Arg
CA9739420
NM_000490.5:c.409G>A
CA310942948
NM_000490.5:c.409G>C