Canonical Allele Identifier: PA2741948046
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2733830
ClinVar RCV Id: RCV003581418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Thr356Ser
CA338442740
NM_014874.4:c.1066A>T
CA338442750
NM_014874.4:c.1067C>G