Canonical Allele Identifier: PA2580110876
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1784152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Thr358Met
CA8120900
NM_000229.2:c.1073C>T