Canonical Allele Identifier: PA2826875512
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1493724
ClinVar RCV Id: RCV001986698 RCV004045417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.His194Arg
CA381551895
NM_001302959.2:c.581A>G