Canonical Allele Identifier: PA2826875499
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1928982
ClinVar RCV Id: RCV002642266 RCV003289564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Glu187Asp
CA381551832
NM_001302959.2:c.561G>T
CA381551833
NM_001302959.2:c.561G>C