Canonical Allele Identifier: PA915998213
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 827274
ClinVar RCV Id: RCV001026851 RCV001039474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Tyr261Cys
CA224165453
NM_003977.4:c.782A>G