Canonical Allele Identifier: PA2826875783
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV003035872
ClinVar Variation:
2127517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.His37Tyr
CA381546306
NM_001302960.2:c.109C>T