Canonical Allele Identifier: PA2826875846
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV002297604
ClinVar Variation:
1717420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Leu62Phe
CA381546843
NM_001302960.2:c.184C>T