Canonical Allele Identifier: PA2580300117
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2452494
ClinVar RCV Id: RCV003172588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp27Glu
CA381545859
NM_003977.4:c.81C>A
CA381545860
NM_003977.4:c.81C>G