Canonical Allele Identifier: PA2573164672
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1447512
ClinVar RCV Id: RCV002011917 RCV002507671 RCV002334959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Gly398Arg
CA8120869
NM_000229.2:c.1192G>A
CA396375500
NM_000229.2:c.1192G>C