Canonical Allele Identifier: PA645407366
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 243057
ClinVar RCV Id: RCV000235088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Val244Leu
CA10584070
NM_014874.4:c.730G>T
CA338438977
NM_014874.4:c.730G>C