Canonical Allele Identifier: PA915998078
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821051
ClinVar RCV Id: RCV001015103 RCV001323868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Val77Met
CA6140754
NM_003977.4:c.229G>A