Canonical Allele Identifier: PA1139672035
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 887805
ClinVar RCV Id: RCV001120751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Ala373Val
CA8120889
NM_000229.2:c.1118C>T