Original source

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

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

Chromosome 4:155510677 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM890186

Most severe consequence
Clinical significance

Synonyms

LSDB 1924

This variation has 5 HGVS names - click the plus to show

4:g.155510677C>A
ENST00000302053.3:c.92G>T
ENSP00000306361.3:p.Gly31Val
ENST00000403106.3:c.92G>T
ENSP00000385981.3:p.Gly31Val

Variation displays