Canonical Allele Identifier: PA2580110819
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1760758
ClinVar RCV Id: RCV002409977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Ile261Phe
CA396376373
NM_000229.2:c.781A>T