Canonical Allele Identifier: PA2499265266
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1064219
ClinVar RCV Id: RCV001374163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Thr79Asn
CA381547166
NM_003977.4:c.236C>A