Canonical Allele Identifier: PA112735
Gene: LCAT HGNC NCBI

Linked Data

ClinVar Variation Id: 3670
ClinVar RCV Id: RCV000003855
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000220.1:p.Thr345Met
CA116425
NM_000229.2:c.1034C>T