Canonical Allele Identifier: CA414820074
Gene: MT-ND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 693631
ClinVar RCV Id: RCV000855009
dbSNP Id: rs1603224410
MyVariant Identifiers: chrMT:g.13913T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13913T>C , J01415.2:m.13913T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1577T>C ENSP00000354813.2:p.Leu526Pro