Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 12:25227346 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM092327, CM061080

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_077_KRAS_190070_0009, 5702, 5691

This variation has 12 HGVS names - click the plus to show

Variation displays