Canonical Allele Identifier: PA916019374
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 485053
ClinVar RCV Id: RCV000565333 RCV000733154 RCV003459374 RCV001554286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Arg69Cys
CA6140795
NM_001302959.2:c.205C>T