Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 17: between 15239508 and 15239509 (forward strand) | View in location tab
with PhenCode IPNMDB_21 (-/C)
LSDB NM_000304.2:c.281dupG, NM_000304.2:c.281_282insG
This variation has 18 HGVS names - click the plus to show
This variant overlaps 8 transcripts.