Canonical Allele Identifier: PA344074
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41166
ClinVar RCV Id: RCV000034065 RCV001012978 RCV001038333
ClinVar Variation Id: 1375499
ClinVar RCV Id: RCV001879696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Lys58Asn
CA344071
NM_003977.4:c.174G>C
CA6140746
NM_003977.4:c.174G>T