Canonical Allele Identifier: PA112612
Gene: LCAT HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Gly57Arg
CA396382170
NM_000229.2:c.169G>C
CA396382173
NM_000229.2:c.169G>A