Canonical Allele Identifier: CA414806291
Gene: MT-ND4L HGNC NCBI

Linked Data

dbSNP Id: rs193302933
MyVariant Identifiers: chrMT:g.10664C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10664C>T , J01415.2:m.10664C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361335.1:c.195C>T ENSP00000354728.1:p.Val65=