Canonical Allele Identifier: CA913179807
Gene:

Linked Data

ClinVar Variation Id: 689934
ClinVar RCV Id: RCV000850787
dbSNP Id: rs1603220015

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5542C>T , J01415.2:m.5542C>T GRCh38