Canonical Allele Identifier: PA2826875501
Gene: AIP HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Tyr189del
CA344175
NM_001302959.2:c.565_567del