Canonical Allele Identifier: PA2825095605
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3066091
ClinVar RCV Id: RCV003991095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Trp315Arg
CA396376011
NM_000229.2:c.943T>C
CA396376012
NM_000229.2:c.943T>A