Canonical Allele Identifier: CA913179990
Gene:

Linked Data

ClinVar Variation Id: 689957
ClinVar RCV Id: RCV000850814
dbSNP Id: rs1603220057

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5608C>T , J01415.2:m.5608C>T GRCh38