Original source

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

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

Chromosome 1:20638104 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM064162

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15641, 2009_August_001_225_PINK1_608309_0011

This variation has 3 HGVS names - click the plus to show

Variation displays