Canonical Allele Identifier: PA2829477342
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 3223608
ClinVar RCV Id: RCV004516372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ile92Phe
CA381547423
NM_003977.4:c.274A>T