Canonical Allele Identifier: CA337096807
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 445420
ClinVar RCV Id: RCV000514068
dbSNP Id: rs368539747
MyVariant Identifiers: chrMT:g.4137C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4137C>T , J01415.2:m.4137C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.831C>T ENSP00000354687.2:p.Tyr277=