Canonical Allele Identifier: PA2580110895
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1764448
ClinVar RCV Id: RCV002373478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Arg423Cys
CA8120862
NM_000229.2:c.1267C>T