Canonical Allele Identifier: PA2573231975
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1499310
ClinVar RCV Id: RCV002010575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Gly31Arg
CA381545883
NM_003977.4:c.91G>A
CA381545885
NM_003977.4:c.91G>C