Canonical Allele Identifier: CA913171825
Gene:

Linked Data

ClinVar Variation Id: 690202
ClinVar RCV Id: RCV000851092
dbSNP Id: rs1603224834

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14690A>G , J01415.2:m.14690A>G GRCh38