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 14:94844898 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920578

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.MET358ARG, 417

This variation has 18 HGVS names - click the plus to show

Variation displays