Allele Registry

Canonical Allele Identifier: PA2573232122

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001870465

ClinVar Variation:

1357170

HGVS (amino-acid)	Matching Registered Transcripts
NP_003968.3:p.Glu197Asp	CA381551023 NM_003977.4:c.591G>T CA381551025 NM_003977.4:c.591G>C