Canonical Allele Identifier: PA2826918793
Gene: LIPG HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294935.1:p.Val377Met
CA8959365
NM_001308006.2:c.1129G>A