Allele Registry

Canonical Allele Identifier: PA2826875394

Gene: AIP HGNC NCBI

ClinVar RCV:

RCV001870465

ClinVar Variation:

1357170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289888.1:p.Glu138Asp	CA381551023 NM_001302959.2:c.414G>T CA381551025 NM_001302959.2:c.414G>C