Allele Registry

Canonical Allele Identifier: PA112624

Gene: LCAT HGNC NCBI

ClinVar RCV:

RCV000003851

ClinVar Variation:

3666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000220.1:p.Leu233Pro	CA116422 NM_000229.2:c.698T>C