Canonical Allele Identifier: PA112576
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 320197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Arg347Cys
CA8120908
NM_000229.2:c.1039C>T