Original source

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

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

Chromosome X:19373511 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM023113

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7529, 2010_April_001_306_PDHA1_300502_0023

This variation has 11 HGVS names - click the plus to show

Variation displays