Canonical Allele Identifier: CA337099688
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs386829181
MyVariant Identifiers: chrMT:g.13437T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13437T>C , J01415.2:m.13437T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361567.2:c.1101T>C ENSP00000354813.2:p.Pro367=
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