Canonical Allele Identifier: CA913163285
Gene:

Linked Data

ClinVar Variation Id: 689838
ClinVar RCV Id: RCV000850668
dbSNP Id: rs1603218586

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1628C>T , J01415.2:m.1628C>T GRCh38