Canonical Allele Identifier: PA2573164673
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1525388
ClinVar RCV Id: RCV002036648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Leu409Pro
CA396375421
NM_000229.2:c.1226T>C