Allele Registry

Canonical Allele Identifier: PA116413

Gene: LCAT HGNC NCBI

ClinVar Allele:

18695

ClinVar RCV:

RCV000003841

ClinVar Variation:

3656

HGVS (amino-acid)	Matching Registered Transcripts
NP_000220.1:p.Trp170Arg	CA116412 NM_000229.2:c.508T>C CA396380025 NM_000229.2:c.508T>A