Canonical Allele Identifier: PA2826876035
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1742518
ClinVar RCV Id: RCV002335286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Val157Met
CA381550222
NM_001302960.2:c.469G>A