Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 12:52952312 (forward strand) | View in location tab
with COSMIC COSM2156487 (G/A)
This variation has 9 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant overlaps 19 transcripts.