Canonical Allele Identifier: PA2829477851
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2837214
ClinVar RCV Id: RCV003692457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala274Phe
CA2739270610
NM_003977.4:c.820_821delinsTT