Canonical Allele Identifier: PA2580300198
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1759691
ClinVar RCV Id: RCV002394191 RCV003099694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.His253Gln
CA6140930
NM_003977.4:c.759C>G
CA381551897
NM_003977.4:c.759C>A