Canonical Allele Identifier: PA2826876144
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 3223622
ClinVar RCV Id: RCV004516386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Ala207Gly
CA381551228
NM_001302960.2:c.620C>G