Canonical Allele Identifier: PA913193798
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 626358
ClinVar RCV Id: RCV000782356
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Met404Val
CA8120867
NM_000229.2:c.1210A>G