Canonical Allele Identifier: PA2826875217
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV002833679
ClinVar Variation:
2008182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Leu11Val
CA381547004
NM_001302959.2:c.31C>G