Canonical Allele Identifier: CA913174699
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693942
ClinVar RCV Id: RCV000855360
dbSNP Id: rs1603225449
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15737G>A , J01415.2:m.15737G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.991G>A ENSP00000354554.2:p.Asp331Asn
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