Canonical Allele Identifier: CA913175224
Gene:

Linked Data

ClinVar Variation Id: 690238
ClinVar RCV Id: RCV000851130
dbSNP Id: rs1603225597

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15926C>T , J01415.2:m.15926C>T GRCh38