Allele Registry

Canonical Allele Identifier: PA112735

Gene: LCAT HGNC NCBI

ClinVar RCV:

RCV000003855

ClinVar Variation:

3670

HGVS (amino-acid)	Matching Registered Transcripts
NP_000220.1:p.Thr345Met	CA116425 NM_000229.2:c.1034C>T