Canonical Allele Identifier: PA2826875893
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1001937
ClinVar RCV Id: RCV001298296 RCV002430093
ClinVar Variation Id: 1017703
ClinVar RCV Id: RCV001316895 RCV003462889 RCV003294272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gln87His
CA381547318
NM_001302960.2:c.261G>C
CA381547319
NM_001302960.2:c.261G>T