Canonical Allele Identifier: PA2580115943
Gene: AVP HGNC NCBI

Linked Data

ClinVar Variation Id: 2443499
ClinVar RCV Id: RCV003152106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000481.2:p.Pro153Leu
CA408061178
NM_000490.5:c.458C>T