Canonical Allele Identifier: CA913171804
Gene:

Linked Data

ClinVar Variation Id: 690199
ClinVar RCV Id: RCV000851089
dbSNP Id: rs1603224828

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14683A>G , J01415.2:m.14683A>G GRCh38