Canonical Allele Identifier: PA2580110830
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2452825
ClinVar RCV Id: RCV003177599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Arg280Cys
CA8120949
NM_000229.2:c.838C>T