Canonical Allele Identifier: PA277614
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217165
ClinVar RCV Id: RCV000201150 RCV000414991 RCV000470638 RCV000857096 RCV001257085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr236Met
CA277612
NM_014874.4:c.707C>T