Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:20644651 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056681

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15640, 2009_August_001_224_PINK1_608309_0010

This variation has 5 HGVS names - click the plus to show

Variation displays