Canonical Allele Identifier: CA913179831
Gene:

Linked Data

ClinVar Variation Id: 689937
ClinVar RCV Id: RCV000850790
dbSNP Id: rs1603220019

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5550C>T , J01415.2:m.5550C>T GRCh38