Canonical Allele Identifier: CA913169479
Gene:

Linked Data

ClinVar Variation Id: 690130
ClinVar RCV Id: RCV000851010
dbSNP Id: rs1603223566

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12142A>G , J01415.2:m.12142A>G GRCh38