Canonical Allele Identifier: PA2580300126
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV003035872
ClinVar Variation:
2127517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.His37Tyr
CA381546306
NM_003977.4:c.109C>T