Canonical Allele Identifier: PA2580110832
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1764100
ClinVar RCV Id: RCV002371172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Val288Met
CA396376194
NM_000229.2:c.862G>A