Canonical Allele Identifier: PA2580192324
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1761202
ClinVar RCV Id: RCV002416706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln261His
CA381554284
NM_001302960.2:c.783A>C
CA381554286
NM_001302960.2:c.783A>T