Canonical Allele Identifier: PA2573259937
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446686
ClinVar RCV Id: RCV001987785 RCV003886538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ala317Ser
CA338441982
NM_014874.4:c.949G>T