Canonical Allele Identifier: PA2741904946
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2566784
ClinVar RCV Id: RCV003306736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp11Tyr
CA381545757
NM_003977.4:c.31G>T