This variation maps to 2 locations

Select a location:
Original source

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

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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.ASP341ASN

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays