Canonical Allele Identifier: CA913171021
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693568
ClinVar RCV Id: RCV000854943
dbSNP Id: rs1603224219
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13524C>A , J01415.2:m.13524C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1188C>A ENSP00000354813.2:p.Ile396=
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