Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 19:17881961 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971393

Most severe consequence
Clinical significance

Synonyms

LSDB 10646

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

19:g.17881961A>C
ENST00000222248.3:c.1060A>C
ENSP00000222248.2:p.Thr354Pro

Variation displays