Canonical Allele Identifier: PA116413
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3656
ClinVar RCV Id: RCV000003841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Trp170Arg
CA116412
NM_000229.2:c.508T>C
CA396380025
NM_000229.2:c.508T>A