Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 4:155507223 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910608

Most severe consequence
Clinical significance

Synonyms

LSDB 1931

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

4:g.155507223C>T
ENST00000302053.3:c.1358G>A
ENSP00000306361.3:p.Ser453Asn
ENST00000403106.3:c.1358G>A
ENSP00000385981.3:p.Ser453Asn

Variation displays