Allele Registry

Canonical Allele Identifier: PA113141

Gene: LIPC HGNC NCBI

ClinVar RCV:

RCV000015537

RCV002054443

ClinVar Variation:

14452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000227.2:p.Ser289Phe	CA210844 NM_000236.3:c.866C>T