Canonical Allele Identifier: CA414774372
Gene: MT-ND1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.4183T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4183T>C , J01415.2:m.4183T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361390.2:c.877T>C ENSP00000354687.2:p.Phe293Leu