Canonical Allele Identifier: PA915970399
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 637737
ClinVar RCV Id: RCV000790031
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Met376Leu
CA338443159
NM_014874.4:c.1126A>C
CA338443169
NM_014874.4:c.1126A>T