Canonical Allele Identifier: PA2580300180
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2000375
ClinVar RCV Id: RCV002797371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Met214del
CA2580084735
NM_003977.4:c.641_643del