Canonical Allele Identifier: PA645505971
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 305729
ClinVar RCV Id: RCV000294654 RCV000733441 RCV000567733 RCV003409472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Glu173Lys
CA6140863
NM_003977.4:c.517G>A