Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 12:25209907 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061830

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5696, 2010_April_001_082_KRAS_190070_0014

This variation has 6 HGVS names - click the plus to show

Variation displays