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 1:20644526 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042450

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_221_PINK1_608309_0004, 15634

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

Variation displays