Canonical Allele Identifier: PA2573232024
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1376671
ClinVar RCV Id: RCV001886062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Gly57Asp
CA381546733
NM_003977.4:c.170G>A