Canonical Allele Identifier: PA2580192288
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1717805
ClinVar RCV Id: RCV002297814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Gly58Asp
CA381549222
NM_001302959.2:c.173G>A