Canonical Allele Identifier: PA2580300139
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV002297604
ClinVar Variation:
1717420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Leu62Phe
CA381546843
NM_003977.4:c.184C>T