Canonical Allele Identifier: PA658678441
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 485052
ClinVar RCV Id: RCV000561910 RCV001054806 RCV000765005 RCV001764674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Arg9Gln
CA6140668
NM_003977.4:c.26G>A