Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 14:23387882 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYH6_4401T_G_022311

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

Variation displays