Canonical Allele Identifier: CA913163346
Gene:

Linked Data

ClinVar Variation Id: 690124
ClinVar RCV Id: RCV000851004
dbSNP Id: rs1603222842

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10456A>G , J01415.2:m.10456A>G GRCh38