Canonical Allele Identifier: PA112535
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3668
ClinVar RCV Id: RCV000003853 RCV002512727
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Arg159Trp
CA116423
NM_000229.2:c.475C>T