Canonical Allele Identifier: CA913169962
Gene:

Linked Data

ClinVar Variation Id: 690183
ClinVar RCV Id: RCV000851070
dbSNP Id: rs1603223647

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12279A>G , J01415.2:m.12279A>G GRCh38