Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:97157179 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 9958

This variation has 3 HGVS names - click the plus to show

8:g.97157179G>T
ENST00000287020.5:c.980C>A
ENSP00000287020.4:p.Pro327His

Variation displays