Canonical Allele Identifier: PA2829477797
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1761202
ClinVar RCV Id: RCV002416706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asn264Thr
CA381554284
NM_003977.4:c.791A>C