Canonical Allele Identifier: PA2825095646
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3230697
ClinVar RCV Id: RCV004522812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Asn408Ser
CA396375428
NM_000229.2:c.1223A>G