Canonical Allele Identifier: PA112624
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3666
ClinVar RCV Id: RCV000003851
JSON-LD

Amino-acid Alleles

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