Canonical Allele Identifier: PA174770
Gene: LONP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161779
ClinVar RCV Id: RCV000149315
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113678.2:p.Leu157Phe
CA174769
NM_031490.5:c.471G>T
CA395828219
NM_031490.5:c.471G>C