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 1:20639952 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042449

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_220_PINK1_608309_0003, 15633

This variation has 4 HGVS names - click the plus to show

Variation displays