Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 14:94844865 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM890098

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.PRO369LEU, 33004

This variation has 18 HGVS names - click the plus to show

Variation displays