Canonical Allele Identifier: CA913180058
Gene:

Linked Data

ClinVar Variation Id: 689961
ClinVar RCV Id: RCV000850818
dbSNP Id: rs1556423015

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5628T>C , J01415.2:m.5628T>C GRCh38