Canonical Allele Identifier: PA112650
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3665
ClinVar RCV Id: RCV000003850
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Met276Lys
CA116421
NM_000229.2:c.827T>A