Canonical Allele Identifier: PA112588
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3659
ClinVar RCV Id: RCV000003844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Asn252Lys
CA116417
NM_000229.2:c.756C>A
CA396376430
NM_000229.2:c.756C>G