Canonical Allele Identifier: PA2826875581
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 822562
ClinVar RCV Id: RCV001018003 RCV003688896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Gln226His
CA381554882
NM_001302959.2:c.678G>C
CA381554885
NM_001302959.2:c.678G>T