Canonical Allele Identifier: PA2829477889
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1394137
ClinVar RCV Id: RCV001898451 RCV002449544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala286Val
CA6140992
NM_003977.4:c.857C>T