Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to Rnor_6.0) (release 138) | View in dbSNP

Alleles
A/G | Ambiguity code: R
Location

This variant has not been mapped

Evidence status

HGVS name

None

About this variant

This variant is mentioned in 1 citation.

Variant displays