Original source

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

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

Chromosome 14:94847443 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012639

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.GLU204LYS, 33002

This variation has 21 HGVS names - click the plus to show

Variation displays