Canonical Allele Identifier: PA2741854385
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2837214
ClinVar RCV Id: RCV003692457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly271Val
CA381554516
NM_001302960.2:c.812G>T
CA2739270610
NM_001302960.2:c.812_813delinsTT