Allele Registry

Canonical Allele Identifier: PA112650

Gene: LCAT HGNC NCBI

ClinVar Allele:

18704

ClinVar RCV:

RCV000003850

ClinVar Variation:

3665

HGVS (amino-acid)	Matching Registered Transcripts
NP_000220.1:p.Met276Lys	CA116421 NM_000229.2:c.827T>A