This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.MET358ARG, 417

HGVS name

None

About this variant

This variant is associated with 4 phenotypes and is mentioned in 4 citations.

Variation displays