Canonical Allele Identifier: PA2826875739
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 305724
ClinVar RCV Id: RCV000304446 RCV000568999 RCV000909790 RCV003920260
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly23Glu
CA6140674
NM_001302960.2:c.68G>A