Canonical Allele Identifier: PA2826875863
Gene: AIP HGNC NCBI
ClinVar RCV:
RCV002833679
ClinVar Variation:
2008182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Leu70Val
CA381547004
NM_001302960.2:c.208C>G